dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.13061285G>T , CM000672.2:g.13061285G>T | GRCh38 |
| NC_000010.10:g.13103285G>T , CM000672.1:g.13103285G>T | GRCh37 |
| NC_000010.9:g.13143291G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378839.1:c.-269-11344C>A | ENSP00000368116.1:n.-269-11344C>A | |
| NM_001282658.1:c.-269-11344C>A | NP_001269587.1:n.-269-11344C>A | |
| NM_001282658.2:c.-269-11344C>A | NP_001269587.1:n.-269-11344C>A |