Linked Data
ClinVar Variation Id:
389634
dbSNP Id:
rs371543989
ExAC:
7:151254321 G / A
gnomAD v2:
7-151254321-G-A
gnomAD v3:
7-151557235-G-A
gnomAD v4:
7-151557235-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151557235G>A , CM000669.2:g.151557235G>A | GRCh38 |
| NC_000007.13:g.151254321G>A , CM000669.1:g.151254321G>A | GRCh37 |
| NC_000007.12:g.150885254G>A | NCBI36 |
| NG_007486.1:g.324996C>T | |
| NG_007486.2:g.324997C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000478989.7:c.*415-3C>T | ENSP00000420645.3:n.*415-3C>T | |
| ENST00000652321.2:c.1676-3C>T | ENSP00000498886.2:n.1676-3C>T | |
| ENST00000287878.9:c.1679-3C>T MANE Select | ENSP00000287878.3:n.1679-3C>T | |
| ENST00000476632.2:c.956-3C>T | ENSP00000419493.2:n.956-3C>T | |
| ENST00000492843.6:c.1304-3C>T | ENSP00000419577.2:n.1304-3C>T | |
| ENST00000650664.1:n.1394-3C>T | ||
| ENST00000650851.1:n.1173-3C>T | ||
| ENST00000650858.1:c.896-3C>T | ENSP00000498384.1:n.896-3C>T | |
| ENST00000650948.1:n.4065-3C>T | ||
| ENST00000651188.1:c.*792-3C>T | ENSP00000498557.1:n.*792-3C>T | |
| ENST00000651303.1:c.*998-3C>T | ENSP00000498428.1:n.*998-3C>T | |
| ENST00000651378.1:c.956-3C>T | ENSP00000499103.1:n.956-3C>T | |
| ENST00000651764.1:c.1547-3C>T | ENSP00000498796.1:n.1547-3C>T | |
| ENST00000651836.1:c.1869-3C>T | ENSP00000499156.1:n.1869-3C>T | |
| ENST00000651954.1:n.1895-3C>T | ||
| ENST00000652047.1:c.1544-3C>T | ENSP00000499111.1:n.1544-3C>T | |
| ENST00000652136.1:n.2226-3C>T | ||
| ENST00000652159.1:c.1547-3C>T | ENSP00000499025.1:n.1547-3C>T | |
| ENST00000652397.1:c.*415-3C>T | ENSP00000498351.1:n.*415-3C>T | |
| ENST00000287878.8:c.1679-3C>T | ENSP00000287878.3:n.1679-3C>T | |
| ENST00000392801.6:c.1547-3C>T | ENSP00000376549.2:n.1547-3C>T | |
| ENST00000418337.6:c.956-3C>T | ENSP00000387386.2:n.956-3C>T | |
| ENST00000479461.1:n.331-3C>T | ||
| ENST00000492843.5:c.1307-3C>T | ENSP00000419577.1:n.1307-3C>T | |
| NM_001040633.1:c.1547-3C>T | NP_001035723.1:n.1547-3C>T | |
| NM_001304527.1:c.1304-3C>T | NP_001291456.1:n.1304-3C>T | |
| NM_001304531.1:c.956-3C>T | NP_001291460.1:n.956-3C>T | |
| NM_016203.3:c.1679-3C>T | NP_057287.2:n.1679-3C>T | |
| NM_024429.1:c.956-3C>T | NP_077747.1:n.956-3C>T | |
| XM_005250002.2:c.*3107C>T | XP_005250059.1:n.*3107C>T | |
| XM_005250004.2:c.*3107C>T | XP_005250061.1:n.*3107C>T | |
| XM_005250006.3:c.*3107C>T | XP_005250063.1:n.*3107C>T | |
| XM_006716021.2:c.*3107C>T | XP_006716084.1:n.*3107C>T | |
| XM_011516282.1:c.*3107C>T | XP_011514584.1:n.*3107C>T | |
| XM_011516283.1:c.1667-3C>T | XP_011514585.1:n.1667-3C>T | |
| XM_011516284.1:c.1664-3C>T | XP_011514586.1:n.1664-3C>T | |
| XM_011516285.1:c.*3107C>T | XP_011514587.1:n.*3107C>T | |
| XM_011516286.1:c.*3107C>T | XP_011514588.1:n.*3107C>T | |
| XM_011516287.1:c.*3107C>T | XP_011514589.1:n.*3107C>T | |
| NM_001363698.1:c.1307-3C>T | NP_001350627.1:n.1307-3C>T | |
| XM_005250002.4:c.*3107C>T | XP_005250059.1:n.*3107C>T | |
| XM_005250004.4:c.*3107C>T | XP_005250061.1:n.*3107C>T | |
| XM_005250006.5:c.*3107C>T | XP_005250063.1:n.*3107C>T | |
| XM_011516285.2:c.*3107C>T | XP_011514587.1:n.*3107C>T | |
| XM_011516286.2:c.*3107C>T | XP_011514588.1:n.*3107C>T | |
| XM_017012268.2:c.*3107C>T | XP_016867757.1:n.*3107C>T | |
| XM_017012269.1:c.1676-3C>T | XP_016867758.1:n.1676-3C>T | |
| XM_017012270.1:c.1547-3C>T | XP_016867759.1:n.1547-3C>T | |
| XM_017012271.2:c.1544-3C>T | XP_016867760.1:n.1544-3C>T | |
| XM_017012272.1:c.1544-3C>T | XP_016867761.1:n.1544-3C>T | |
| XM_017012274.2:c.*3107C>T | XP_016867763.1:n.*3107C>T | |
| XM_017012275.2:c.*3107C>T | XP_016867764.1:n.*3107C>T | |
| XM_017012276.2:c.953-3C>T | XP_016867765.1:n.953-3C>T | |
| XM_017012277.2:c.932-3C>T | XP_016867766.1:n.932-3C>T | |
| XM_017012278.1:c.896-3C>T | XP_016867767.1:n.896-3C>T | |
| XM_017012279.2:c.896-3C>T | XP_016867768.1:n.896-3C>T | |
| XM_017012280.2:c.896-3C>T | XP_016867769.1:n.896-3C>T | |
| XM_017012281.2:c.896-3C>T | XP_016867770.1:n.896-3C>T | |
| XM_024446786.1:c.*3107C>T | XP_024302554.1:n.*3107C>T | |
| XM_024446787.1:c.*3107C>T | XP_024302555.1:n.*3107C>T | |
| XM_024446788.1:c.*3107C>T | XP_024302556.1:n.*3107C>T | |
| XM_024446789.1:c.956-3C>T | XP_024302557.1:n.956-3C>T | |
| NM_016203.4:c.1679-3C>T MANE Select | NP_057287.2:n.1679-3C>T | |
| NM_001040633.2:c.1547-3C>T | NP_001035723.1:n.1547-3C>T | |
| NM_001304527.2:c.1304-3C>T | NP_001291456.1:n.1304-3C>T | |
| NM_001304531.2:c.956-3C>T | NP_001291460.1:n.956-3C>T | |
| NM_001363698.2:c.1307-3C>T | NP_001350627.1:n.1307-3C>T | |
| NM_024429.2:c.956-3C>T | NP_077747.1:n.956-3C>T |