dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38080367T>G , CM000664.2:g.38080367T>G | GRCh38 |
| NC_000002.11:g.38307509T>G , CM000664.1:g.38307509T>G | GRCh37 |
| NC_000002.10:g.38161013T>G | NCBI36 |
| NG_008386.2:g.735A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494864.1:c.-70-9057A>C | ENSP00000479876.1:n.-70-9057A>C | |
| XM_011533236.1:c.1174+3807T>G | XP_011531538.1:n.1174+3807T>G |