Linked Data
dbSNP Id:
rs2120461
gnomAD v2:
1-8447722-C-T
gnomAD v3:
1-8387662-C-T
gnomAD v4:
1-8387662-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.8387662C>T , CM000663.2:g.8387662C>T | GRCh38 |
| NC_000001.10:g.8447722C>T , CM000663.1:g.8447722C>T | GRCh37 |
| NC_000001.9:g.8370309C>T | NCBI36 |
| NG_047035.1:g.435030G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000465125.2:c.-378-21688G>A | ENSP00000515651.1:n.-378-21688G>A | |
| ENST00000400908.7:c.1285-21688G>A MANE Select | ENSP00000383700.2:n.1285-21688G>A | |
| ENST00000656437.1:c.1285-21688G>A | ENSP00000499322.1:n.1285-21688G>A | |
| ENST00000337907.7:c.1285-21688G>A | ENSP00000338629.3:n.1285-21688G>A | |
| ENST00000377464.5:c.481-21688G>A | ENSP00000366684.1:n.481-21688G>A | |
| ENST00000400907.6:c.1285-21688G>A | ENSP00000383699.2:n.1285-21688G>A | |
| ENST00000400908.6:c.1285-21688G>A | ENSP00000383700.2:n.1285-21688G>A | |
| ENST00000460659.5:n.335-21688G>A | ||
| ENST00000465125.1:n.302-21688G>A | ||
| ENST00000476556.5:c.-378-21688G>A | ENSP00000422246.1:n.-378-21688G>A | |
| ENST00000488215.5:c.-378-21688G>A | ENSP00000464847.1:n.-378-21688G>A | |
| ENST00000492766.5:n.269-21688G>A | ||
| NM_001042681.1:c.1285-21688G>A | NP_001036146.1:n.1285-21688G>A | |
| NM_001042682.1:c.-378-21688G>A | NP_001036147.1:n.-378-21688G>A | |
| NM_012102.3:c.1285-21688G>A | NP_036234.3:n.1285-21688G>A | |
| XM_005263464.1:c.1285-21688G>A | XP_005263521.1:n.1285-21688G>A | |
| XM_005263466.1:c.481-21688G>A | XP_005263523.1:n.481-21688G>A | |
| XM_006710653.1:c.1285-21688G>A | XP_006710716.1:n.1285-21688G>A | |
| XM_011541510.1:c.1159-21688G>A | XP_011539812.1:n.1159-21688G>A | |
| XM_011541511.1:c.1285-21688G>A | XP_011539813.1:n.1285-21688G>A | |
| XM_005263464.2:c.1285-21688G>A | XP_005263521.1:n.1285-21688G>A | |
| XM_011541510.2:c.1159-21688G>A | XP_011539812.1:n.1159-21688G>A | |
| XM_011541511.2:c.1285-21688G>A | XP_011539813.1:n.1285-21688G>A | |
| XM_017001358.1:c.1285-21688G>A | XP_016856847.1:n.1285-21688G>A | |
| XM_017001359.1:c.1285-21688G>A | XP_016856848.1:n.1285-21688G>A | |
| NM_001042681.2:c.1285-21688G>A MANE Select | NP_001036146.1:n.1285-21688G>A | |
| NM_001042682.2:c.-378-21688G>A | NP_001036147.1:n.-378-21688G>A | |
| NM_012102.4:c.1285-21688G>A | NP_036234.3:n.1285-21688G>A |