Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.100646272C>G , CM000669.2:g.100646272C>G | GRCh38 |
| NC_000007.13:g.100243895C>G , CM000669.1:g.100243895C>G | GRCh37 |
| NC_000007.12:g.100081831C>G | NCBI36 |
| NG_007989.1:g.279G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_016188.5:c.1177G>C MANE Select | NP_057272.1:p.Gly393Arg |
| ENST00000160382.10:c.1177G>C MANE Select | ENSP00000160382.5:p.Gly393Arg |
| NM_016188.4:c.1177G>C | NP_057272.1:p.Gly393Arg |
| NR_134539.1:n.1301G>C | |
| NR_134539.2:n.1288G>C | |
| ENST00000160382.9:c.1177G>C | ENSP00000160382.5:p.Gly393Arg |
| ENST00000487125.1:n.739G>C | |
| XR_927476.1:n.1301G>C |