HGVS | Genome Assembly |
---|---|
NC_000009.12:g.114785336T= , CM000671.2:g.114785336T= | GRCh38 |
NC_000009.11:g.117547616T= , CM000671.1:g.117547616T= | GRCh37 |
NC_000009.10:g.116587437T= | NCBI36 |
NG_011488.2:g.25793A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374045.5:c.*5116A= MANE Select | ENSP00000363157.3:n.*5116A= | |
ENST00000374045.4:c.*5116A= | ENSP00000363157.3:n.*5116A= | |
NM_001204344.1:c.5695A= | NP_001191273.1:n.5695A= | |
NM_005118.3:c.*5116A= | NP_005109.2:n.*5116A= | |
NM_005118.4:c.*5116A= MANE Select | NP_005109.2:n.*5116A= |