dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31168676A>T , CM000668.2:g.31168676A>T | GRCh38 |
| NC_000006.11:g.31136453A>T , CM000668.1:g.31136453A>T | GRCh37 |
| NC_000006.10:g.31244432A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259915.13:c.405+1540T>A MANE Select | ENSP00000259915.7:n.405+1540T>A | |
| ENST00000259915.12:c.405+1540T>A | ENSP00000259915.7:n.405+1540T>A | |
| ENST00000441888.7:c.-183-2629T>A | ENSP00000389359.2:n.-183-2629T>A | |
| ENST00000461401.1:n.443+1540T>A | ||
| ENST00000619340.1:c.405+1540T>A | ENSP00000481679.1:n.405+1540T>A | |
| NM_002701.5:c.405+1540T>A | NP_002692.2:n.405+1540T>A | |
| NM_002701.6:c.405+1540T>A MANE Select | NP_002692.2:n.405+1540T>A |