dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23507801A>T , CM000676.2:g.23507801A>T | GRCh38 |
| NC_000014.8:g.23977010A>T , CM000676.1:g.23977010A>T | GRCh37 |
| NC_000014.7:g.23046850A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000556699.2:c.929-1539A>T | ENSP00000451942.2:n.929-1539A>T | |
| ENST00000703257.1:c.871-1539A>T | ENSP00000515246.1:n.871-1539A>T | |
| ENST00000556699.1:c.203-1539A>T | ENSP00000451942.1:n.203-1539A>T |