HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488548A>G , CM000674.2:g.52488548A>G | GRCh38 |
NC_000012.11:g.52882332A>G , CM000674.1:g.52882332A>G | GRCh37 |
NC_000012.10:g.51168599A>G | NCBI36 |
NG_008298.1:g.9850T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1204T>C MANE Select | ENSP00000369317.3:p.Cys402Arg | |
ENST00000330722.6:c.1204T>C | ENSP00000369317.3:p.Cys402Arg | |
NM_005554.3:c.1204T>C | NP_005545.1:p.Cys402Arg | |
NM_005554.4:c.1204T>C MANE Select | NP_005545.1:p.Cys402Arg |