Linked Data
dbSNP Id:
rs776869938
ExAC:
2:1499723 A / G
gnomAD v2:
2-1499723-A-G
gnomAD v4:
2-1495951-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.1495951A>G , CM000664.2:g.1495951A>G | GRCh38 |
| NC_000002.11:g.1499723A>G , CM000664.1:g.1499723A>G | GRCh37 |
| NC_000002.10:g.1478730A>G | NCBI36 |
| NG_011581.1:g.87489A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329066.9:c.2007-38A>G MANE Select | ENSP00000329869.4:n.2007-38A>G | |
| ENST00000329066.8:c.2007-38A>G | ENSP00000329869.4:n.2007-38A>G | |
| ENST00000345913.8:c.2007-38A>G | ENSP00000318820.7:n.2007-38A>G | |
| ENST00000346956.7:c.2007-38A>G | ENSP00000263886.6:n.2007-38A>G | |
| ENST00000382198.5:c.1488-38A>G | ENSP00000371633.1:n.1488-38A>G | |
| ENST00000382201.7:c.1836-38A>G | ENSP00000371636.3:n.1836-38A>G | |
| ENST00000422464.5:c.1794-38A>G | ENSP00000405788.1:n.1794-38A>G | |
| ENST00000446278.5:c.431-38A>G | ||
| ENST00000462973.5:n.424+1912A>G | ||
| ENST00000469607.3:c.429-38A>G | ENSP00000419461.1:n.429-38A>G | |
| ENST00000497517.6:n.677+1912A>G | ||
| NM_000547.5:c.2007-38A>G | NP_000538.3:n.2007-38A>G | |
| NM_001206744.1:c.2007-38A>G | NP_001193673.1:n.2007-38A>G | |
| NM_001206745.1:c.1836-38A>G | NP_001193674.1:n.1836-38A>G | |
| NM_175719.3:c.1836-38A>G | NP_783650.1:n.1836-38A>G | |
| NM_175721.3:c.2007-38A>G | NP_783652.1:n.2007-38A>G | |
| NM_175722.3:c.1488-38A>G | NP_783653.1:n.1488-38A>G | |
| XM_011510379.1:c.2007-38A>G | XP_011508681.1:n.2007-38A>G | |
| XM_011510380.1:c.2007-38A>G | XP_011508682.1:n.2007-38A>G | |
| XM_011510381.1:c.1836-38A>G | XP_011508683.1:n.1836-38A>G | |
| XR_922681.1:n.2008-38A>G | ||
| XM_011510380.3:c.2043-38A>G | XP_011508682.2:n.2043-38A>G | |
| XM_024453085.1:c.2043-38A>G | XP_024308853.1:n.2043-38A>G | |
| XM_024453086.1:c.2043-38A>G | XP_024308854.1:n.2043-38A>G | |
| XM_024453087.1:c.2007-38A>G | XP_024308855.1:n.2007-38A>G | |
| XM_024453088.1:c.2007-38A>G | XP_024308856.1:n.2007-38A>G | |
| XM_024453089.1:c.2007-38A>G | XP_024308857.1:n.2007-38A>G | |
| XM_024453090.1:c.2043-38A>G | XP_024308858.1:n.2043-38A>G | |
| XM_024453091.1:c.1872-38A>G | XP_024308859.1:n.1872-38A>G | |
| XM_024453092.1:c.1872-38A>G | XP_024308860.1:n.1872-38A>G | |
| XM_024453093.1:c.1524-38A>G | XP_024308861.1:n.1524-38A>G | |
| NM_001206744.2:c.2007-38A>G MANE Select | NP_001193673.1:n.2007-38A>G | |
| NM_000547.6:c.2007-38A>G | NP_000538.3:n.2007-38A>G | |
| NM_001206745.2:c.1836-38A>G | NP_001193674.1:n.1836-38A>G | |
| NM_175719.4:c.1836-38A>G | NP_783650.1:n.1836-38A>G |