HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827628T>G , CM000667.2:g.148827628T>G | GRCh38 |
NC_000005.9:g.148207191T>G , CM000667.1:g.148207191T>G | GRCh37 |
NC_000005.8:g.148187384T>G | NCBI36 |
NG_016421.1:g.6036T>G | |
NG_016421.2:g.6036T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.797T>G MANE Select | ENSP00000305372.4:p.Leu266Trp | |
ENST00000305988.5:c.797T>G | ENSP00000305372.4:p.Leu266Trp | |
NM_000024.5:c.797T>G | NP_000015.1:p.Leu266Trp | |
NM_000024.6:c.797T>G MANE Select | NP_000015.2:p.Leu266Trp |