HGVS | Genome Assembly |
---|---|
NC_000016.10:g.84031946A>C , CM000678.2:g.84031946A>C | GRCh38 |
NC_000016.9:g.84065551A>C , CM000678.1:g.84065551A>C | GRCh37 |
NC_000016.8:g.82623052A>C | NCBI36 |
NG_034136.1:g.15212T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299709.8:c.553T>G MANE Select | ENSP00000299709.3:p.Cys185Gly | |
ENST00000299709.7:c.553T>G | ENSP00000299709.3:p.Cys185Gly | |
ENST00000568178.1:c.553T>G | ENSP00000457737.1:p.Cys185Gly | |
NM_001080442.2:c.553T>G | NP_001073911.1:p.Cys185Gly | |
XM_011522872.1:c.553T>G | XP_011521174.1:p.Cys185Gly | |
XM_017022946.1:c.553T>G | XP_016878435.1:p.Cys185Gly | |
NM_001080442.3:c.553T>G MANE Select | NP_001073911.1:p.Cys185Gly |