HGVS | Genome Assembly |
---|---|
NC_000005.10:g.146339929G>T , CM000667.2:g.146339929G>T | GRCh38 |
NC_000005.9:g.145719492G>T , CM000667.1:g.145719492G>T | GRCh37 |
NC_000005.8:g.145699685G>T | NCBI36 |
NG_011885.1:g.5906G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000646991.2:c.502G>T MANE Select | ENSP00000495718.1:p.Ala168Ser | |
ENST00000230732.4:c.502G>T | ENSP00000230732.4:p.Ala168Ser | |
NM_002700.2:c.502G>T | NP_002691.1:p.Ala168Ser | |
NM_002700.3:c.502G>T MANE Select | NP_002691.1:p.Ala168Ser |