HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367802C>G , CM000677.2:g.73367802C>G | GRCh38 |
NC_000015.9:g.73660143C>G , CM000677.1:g.73660143C>G | GRCh37 |
NC_000015.8:g.71447196C>G | NCBI36 |
NG_009063.1:g.6463G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.469G>C MANE Select | ENSP00000261917.3:p.Ala157Pro | |
ENST00000261917.3:c.469G>C | ENSP00000261917.3:p.Ala157Pro | |
NM_005477.2:c.469G>C | NP_005468.1:p.Ala157Pro | |
NM_005477.3:c.469G>C MANE Select | NP_005468.1:p.Ala157Pro |