Linked Data
ClinVar Variation Id:
292768
dbSNP Id:
rs376867928
ExAC:
1:154569591 C / T
gnomAD v2:
1-154569591-C-T
gnomAD v3:
1-154597115-C-T
gnomAD v4:
1-154597115-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154597115C>T , CM000663.2:g.154597115C>T | GRCh38 |
| NC_000001.10:g.154569591C>T , CM000663.1:g.154569591C>T | GRCh37 |
| NC_000001.9:g.152836215C>T | NCBI36 |
| NG_011844.1:g.35847G>A | |
| NG_011844.2:g.39446G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649042.2:c.1973+8G>A | ENSP00000497790.2:n.1973+8G>A | |
| ENST00000649724.2:c.2109+8G>A | ENSP00000497932.2:n.2109+8G>A | |
| ENST00000680270.2:c.1962+8G>A | ENSP00000505532.2:n.1962+8G>A | |
| ENST00000681056.2:c.1731+8G>A | ENSP00000506234.2:n.1731+8G>A | |
| ENST00000368471.8:c.1194+8G>A | ENSP00000357456.3:n.1194+8G>A | |
| ENST00000368474.9:c.2079+8G>A MANE Select | ENSP00000357459.4:n.2079+8G>A | |
| ENST00000529168.2:c.2079+8G>A | ENSP00000431794.2:n.2079+8G>A | |
| ENST00000647682.2:n.1809+8G>A | ||
| ENST00000648231.2:c.1194+8G>A | ENSP00000497555.1:n.1194+8G>A | |
| ENST00000648311.1:c.1194+8G>A | ENSP00000498137.1:n.1194+8G>A | |
| ENST00000648714.2:c.2079+8G>A | ENSP00000497434.2:n.2079+8G>A | |
| ENST00000649021.1:n.2115+8G>A | ||
| ENST00000649022.2:c.1194+8G>A | ENSP00000496896.2:n.1194+8G>A | |
| ENST00000649042.1:c.1194+8G>A | ENSP00000497790.1:n.1194+8G>A | |
| ENST00000649408.2:c.2079+8G>A | ENSP00000497386.2:n.2079+8G>A | |
| ENST00000649724.1:c.1194+8G>A | ENSP00000497932.1:n.1194+8G>A | |
| ENST00000649749.1:c.1194+8G>A | ENSP00000497210.1:n.1194+8G>A | |
| ENST00000679375.1:c.*389+8G>A | ENSP00000505887.1:n.*389+8G>A | |
| ENST00000679465.1:n.2277+8G>A | ||
| ENST00000679805.1:n.2115+8G>A | ||
| ENST00000679899.1:c.1194+8G>A | ENSP00000505996.1:n.1194+8G>A | |
| ENST00000680270.1:c.1194+8G>A | ENSP00000505532.1:n.1194+8G>A | |
| ENST00000680305.1:c.2079+8G>A | ENSP00000506312.1:n.2079+8G>A | |
| ENST00000681056.1:c.1194+8G>A | ENSP00000506234.1:n.1194+8G>A | |
| ENST00000681235.1:c.*1679+8G>A | ENSP00000506606.1:n.*1679+8G>A | |
| ENST00000681429.1:n.1339+8G>A | ||
| ENST00000681683.1:c.1194+8G>A | ENSP00000506666.1:n.1194+8G>A | |
| ENST00000681786.1:n.2277+8G>A | ||
| ENST00000681901.1:c.*1679+8G>A | ENSP00000504883.1:n.*1679+8G>A | |
| ENST00000368471.7:c.1194+8G>A | ENSP00000357456.3:n.1194+8G>A | |
| ENST00000368474.8:c.2079+8G>A | ENSP00000357459.4:n.2079+8G>A | |
| ENST00000529168.1:c.2064+8G>A | ENSP00000431794.1:n.2064+8G>A | |
| NM_001025107.2:c.1194+8G>A | NP_001020278.1:n.1194+8G>A | |
| NM_001111.4:c.2079+8G>A | NP_001102.2:n.2079+8G>A | |
| NM_001193495.1:c.1194+8G>A | NP_001180424.1:n.1194+8G>A | |
| NM_015840.3:c.2079+8G>A | NP_056655.2:n.2079+8G>A | |
| NM_015841.3:c.2079+8G>A | NP_056656.2:n.2079+8G>A | |
| XM_006711109.1:c.2109+8G>A | XP_006711172.1:n.2109+8G>A | |
| XM_006711111.2:c.1194+8G>A | XP_006711174.1:n.1194+8G>A | |
| XM_006711112.1:c.1194+8G>A | XP_006711175.1:n.1194+8G>A | |
| XM_006711113.1:c.1194+8G>A | XP_006711176.1:n.1194+8G>A | |
| XM_011509060.1:c.2208+8G>A | XP_011507362.1:n.2208+8G>A | |
| XM_011509061.1:c.2208+8G>A | XP_011507363.1:n.2208+8G>A | |
| XM_011509062.1:c.2097+8G>A | XP_011507364.1:n.2097+8G>A | |
| NM_001025107.3:c.1194+8G>A | NP_001020278.1:n.1194+8G>A | |
| NM_001111.5:c.2079+8G>A MANE Select | NP_001102.3:n.2079+8G>A | |
| NM_001193495.2:c.1194+8G>A | NP_001180424.1:n.1194+8G>A | |
| NM_001365045.1:c.2106+8G>A | NP_001351974.1:n.2106+8G>A | |
| NM_001365046.1:c.1194+8G>A | NP_001351975.1:n.1194+8G>A | |
| NM_001365047.1:c.1194+8G>A | NP_001351976.1:n.1194+8G>A | |
| NM_001365048.1:c.1194+8G>A | NP_001351977.1:n.1194+8G>A | |
| NM_001365049.1:c.1194+8G>A | NP_001351978.1:n.1194+8G>A | |
| NM_015840.4:c.2079+8G>A | NP_056655.3:n.2079+8G>A | |
| NM_015841.4:c.2079+8G>A | NP_056656.3:n.2079+8G>A | |
| XM_006711113.2:c.1194+8G>A | XP_006711176.1:n.1194+8G>A | |
| XM_011509061.2:c.1194+8G>A | XP_011507363.2:n.1194+8G>A | |
| XM_024449674.1:c.2208+8G>A | XP_024305442.1:n.2208+8G>A |