HGVS | Genome Assembly |
---|---|
NC_000005.10:g.154477515T>A , CM000667.2:g.154477515T>A | GRCh38 |
NC_000005.9:g.153857075T>A , CM000667.1:g.153857075T>A | GRCh37 |
NC_000005.8:g.153837268T>A | NCBI36 |
NG_052889.1:g.5750A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000231121.3:c.494A>T MANE Select | ENSP00000231121.2:p.Glu165Val | |
ENST00000231121.2:c.494A>T | ENSP00000231121.2:p.Glu165Val | |
NM_004821.2:c.494A>T | NP_004812.1:p.Glu165Val | |
XM_005268531.1:c.494A>T | XP_005268588.1:p.Glu165Val | |
NM_004821.3:c.494A>T MANE Select | NP_004812.1:p.Glu165Val |