HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436008C>G , CM000678.2:g.67436008C>G | GRCh38 |
NC_000016.9:g.67469911C>G , CM000678.1:g.67469911C>G | GRCh37 |
NC_000016.8:g.66027412C>G | NCBI36 |
NG_016549.1:g.9876C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.530C>G MANE Select | ENSP00000316786.5:p.Ala177Gly | |
ENST00000326152.5:c.530C>G | ENSP00000316786.5:p.Ala177Gly | |
ENST00000566606.1:c.508C>G | ENSP00000473429.1:n.508C>G | |
ENST00000567684.2:n.393C>G | ||
NM_000196.3:c.530C>G | NP_000187.3:p.Ala177Gly | |
NM_000196.4:c.530C>G MANE Select | NP_000187.3:p.Ala177Gly |