HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011215A>C , CM000682.2:g.46011215A>C | GRCh38 |
NC_000020.10:g.44639854A>C , CM000682.1:g.44639854A>C | GRCh37 |
NC_000020.9:g.44073261A>C | NCBI36 |
NG_011468.1:g.7308A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.722A>C MANE Select | ENSP00000361405.3:p.Tyr241Ser | |
NM_004994.2:c.722A>C | NP_004985.2:p.Tyr241Ser | |
NM_004994.3:c.722A>C MANE Select | NP_004985.2:p.Tyr241Ser |