Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5985617A>G , CM000674.2:g.5985617A>G | GRCh38 |
| NC_000012.11:g.6094783A>G , CM000674.1:g.6094783A>G | GRCh37 |
| NC_000012.10:g.5965044A>G | NCBI36 |
| NG_009072.1:g.144054T>C | |
| NG_009072.2:g.144054T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000552.5:c.6847T>C MANE Select | NP_000543.3:p.Cys2283Arg |
| ENST00000261405.10:c.6847T>C MANE Select | ENSP00000261405.5:p.Cys2283Arg |
| NM_000552.3:c.6847T>C | NP_000543.2:p.Cys2283Arg |
| NM_000552.4:c.6847T>C | NP_000543.2:p.Cys2283Arg |
| ENST00000261405.9:c.6847T>C | ENSP00000261405.5:p.Cys2283Arg |