HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488409T>C , CM000674.2:g.52488409T>C | GRCh38 |
NC_000012.11:g.52882193T>C , CM000674.1:g.52882193T>C | GRCh37 |
NC_000012.10:g.51168460T>C | NCBI36 |
NG_008298.1:g.9989A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1343A>G MANE Select | ENSP00000369317.3:p.Tyr448Cys | |
ENST00000330722.6:c.1343A>G | ENSP00000369317.3:p.Tyr448Cys | |
NM_005554.3:c.1343A>G | NP_005545.1:p.Tyr448Cys | |
NM_005554.4:c.1343A>G MANE Select | NP_005545.1:p.Tyr448Cys |