Linked Data
ClinVar Variation Id:
360659
dbSNP Id:
rs150404125
ExAC:
7:73477642 G / A
gnomAD v2:
7-73477642-G-A
gnomAD v3:
7-74063312-G-A
gnomAD v4:
7-74063312-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.74063312G>A , CM000669.2:g.74063312G>A | GRCh38 |
| NC_000007.13:g.73477642G>A , CM000669.1:g.73477642G>A | GRCh37 |
| NC_000007.12:g.73115578G>A | NCBI36 |
| NG_009261.1:g.40216G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000692049.1:c.2047G>A | ENSP00000510104.1:p.Ala683Thr | |
| ENST00000252034.12:c.1861G>A MANE Select | ENSP00000252034.7:p.Ala621Thr | |
| ENST00000252034.11:c.1861G>A | ENSP00000252034.7:p.Ala621Thr | |
| ENST00000320399.10:c.1960G>A | ENSP00000313565.6:p.Ala654Thr | |
| ENST00000320492.11:c.1618G>A | ENSP00000315607.7:p.Ala540Thr | |
| ENST00000357036.9:c.1876G>A | ENSP00000349540.5:p.Ala626Thr | |
| ENST00000358929.8:c.2047G>A | ENSP00000351807.5:p.Ala683Thr | |
| ENST00000380553.8:c.1453G>A | ENSP00000369926.4:p.Ala485Thr | |
| ENST00000380562.8:c.1879G>A | ENSP00000369936.4:p.Ala627Thr | |
| ENST00000380575.8:c.1774G>A | ENSP00000369949.4:p.Ala592Thr | |
| ENST00000380576.9:c.1804G>A | ENSP00000369950.5:p.Ala602Thr | |
| ENST00000380584.8:c.1717G>A | ENSP00000369958.4:p.Ala573Thr | |
| ENST00000414324.5:c.1789G>A | ENSP00000392575.1:p.Ala597Thr | |
| ENST00000429192.5:c.1819G>A | ENSP00000391129.1:p.Ala607Thr | |
| ENST00000445912.5:c.1861G>A | ENSP00000389857.1:p.Ala621Thr | |
| ENST00000458204.5:c.1831G>A | ENSP00000403162.1:p.Ala611Thr | |
| ENST00000621115.4:c.1594G>A | ENSP00000480955.1:p.Ala532Thr | |
| NM_000501.3:c.1861G>A | NP_000492.2:p.Ala621Thr | |
| NM_001081752.2:c.1774G>A | NP_001075221.1:p.Ala592Thr | |
| NM_001081753.2:c.1819G>A | NP_001075222.1:p.Ala607Thr | |
| NM_001081754.2:c.1876G>A | NP_001075223.1:p.Ala626Thr | |
| NM_001081755.2:c.1804G>A | NP_001075224.1:p.Ala602Thr | |
| NM_001278912.1:c.1861G>A | NP_001265841.1:p.Ala621Thr | |
| NM_001278913.1:c.1618G>A | NP_001265842.1:p.Ala540Thr | |
| NM_001278914.1:c.1789G>A | NP_001265843.1:p.Ala597Thr | |
| NM_001278915.1:c.1879G>A | NP_001265844.1:p.Ala627Thr | |
| NM_001278916.1:c.1717G>A | NP_001265845.1:p.Ala573Thr | |
| NM_001278917.1:c.1831G>A | NP_001265846.1:p.Ala611Thr | |
| NM_001278918.1:c.1594G>A | NP_001265847.1:p.Ala532Thr | |
| NM_001278939.1:c.2047G>A | NP_001265868.1:p.Ala683Thr | |
| XM_005250187.1:c.1825G>A | XP_005250244.1:p.Ala609Thr | |
| XM_005250188.1:c.1819G>A | XP_005250245.1:p.Ala607Thr | |
| XM_011515868.1:c.1876G>A | XP_011514170.1:p.Ala626Thr | |
| XM_011515869.1:c.1846G>A | XP_011514171.1:p.Ala616Thr | |
| XM_011515870.1:c.1840G>A | XP_011514172.1:p.Ala614Thr | |
| XM_011515871.1:c.1834G>A | XP_011514173.1:p.Ala612Thr | |
| XM_011515872.1:c.1822G>A | XP_011514174.1:p.Ala608Thr | |
| XM_011515873.1:c.1819G>A | XP_011514175.1:p.Ala607Thr | |
| XM_011515874.1:c.1810G>A | XP_011514176.1:p.Ala604Thr | |
| XM_011515875.1:c.1795G>A | XP_011514177.1:p.Ala599Thr | |
| XM_011515876.1:c.1876G>A | XP_011514178.1:p.Ala626Thr | |
| XM_011515877.1:c.1765G>A | XP_011514179.1:p.Ala589Thr | |
| XM_005250187.2:c.1825G>A | XP_005250244.1:p.Ala609Thr | |
| XM_005250188.2:c.1819G>A | XP_005250245.1:p.Ala607Thr | |
| XM_011515868.2:c.1876G>A | XP_011514170.1:p.Ala626Thr | |
| XM_011515871.2:c.1834G>A | XP_011514173.1:p.Ala612Thr | |
| XM_011515872.2:c.1822G>A | XP_011514174.1:p.Ala608Thr | |
| XM_011515873.2:c.1819G>A | XP_011514175.1:p.Ala607Thr | |
| XM_011515875.2:c.1795G>A | XP_011514177.1:p.Ala599Thr | |
| XM_011515876.2:c.1876G>A | XP_011514178.1:p.Ala626Thr | |
| XM_011515877.2:c.1765G>A | XP_011514179.1:p.Ala589Thr | |
| XM_017011813.1:c.1789G>A | XP_016867302.1:p.Ala597Thr | |
| XM_017011814.2:c.1777G>A | XP_016867303.1:p.Ala593Thr | |
| NM_000501.4:c.1861G>A MANE Select | NP_000492.2:p.Ala621Thr | |
| NM_001081752.3:c.1774G>A | NP_001075221.1:p.Ala592Thr | |
| NM_001081753.3:c.1819G>A | NP_001075222.1:p.Ala607Thr | |
| NM_001081754.3:c.1876G>A | NP_001075223.1:p.Ala626Thr | |
| NM_001081755.3:c.1804G>A | NP_001075224.1:p.Ala602Thr | |
| NM_001278912.2:c.1861G>A | NP_001265841.1:p.Ala621Thr | |
| NM_001278913.2:c.1618G>A | NP_001265842.1:p.Ala540Thr | |
| NM_001278914.2:c.1789G>A | NP_001265843.1:p.Ala597Thr | |
| NM_001278915.2:c.1879G>A | NP_001265844.1:p.Ala627Thr | |
| NM_001278916.2:c.1717G>A | NP_001265845.1:p.Ala573Thr | |
| NM_001278917.2:c.1831G>A | NP_001265846.1:p.Ala611Thr | |
| NM_001278918.2:c.1594G>A | NP_001265847.1:p.Ala532Thr | |
| NM_001278939.2:c.2047G>A | NP_001265868.1:p.Ala683Thr |