dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24273563G>T , CM000668.2:g.24273563G>T | GRCh38 |
| NC_000006.11:g.24273791G>T , CM000668.1:g.24273791G>T | GRCh37 |
| NC_000006.10:g.24381770G>T | NCBI36 |
| NG_012829.1:g.89490C>A | |
| NG_012829.2:g.114730C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.922+4486C>A MANE Select | ENSP00000367715.3:n.922+4486C>A | |
| ENST00000378454.7:c.922+4486C>A | ENSP00000367715.3:n.922+4486C>A | |
| NM_001195610.1:c.922+4486C>A | NP_001182539.1:n.922+4486C>A | |
| NM_016356.4:c.922+4486C>A | NP_057440.2:n.922+4486C>A | |
| NM_016356.5:c.922+4486C>A MANE Select | NP_057440.2:n.922+4486C>A | |
| NM_001195610.2:c.922+4486C>A | NP_001182539.1:n.922+4486C>A |