dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.107885825G>T , CM000673.2:g.107885825G>T | GRCh38 |
| NC_000011.9:g.107756551G>T , CM000673.1:g.107756551G>T | GRCh37 |
| NC_000011.8:g.107261761G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525071.5:c.-349+22616C>A | ENSP00000434307.1:n.-349+22616C>A |