Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12710200C>T , CM000686.2:g.12710200C>T | GRCh38 |
| NC_000024.9:g.14822133C>T , CM000686.1:g.14822133C>T | GRCh37 |
| NC_000024.8:g.13331527C>T | NCBI36 |
| NG_008311.1:g.13974C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651177.1:c.96+657C>T | ENSP00000498372.1:n.96+657C>T | |
| ENST00000338981.7:c.96+657C>T MANE Select | ENSP00000342812.3:n.96+657C>T | |
| ENST00000426564.6:n.108+657C>T | ||
| ENST00000493168.1:n.172+657C>T | ||
| NM_004654.3:c.96+657C>T | NP_004645.2:n.96+657C>T | |
| XM_011531469.1:c.96+657C>T | XP_011529771.1:n.96+657C>T | |
| XM_017030078.2:c.96+657C>T | XP_016885567.1:n.96+657C>T | |
| NM_004654.4:c.96+657C>T MANE Select | NP_004645.2:n.96+657C>T |