HGVS | Genome Assembly |
---|---|
NC_000002.12:g.46306152T= , CM000664.2:g.46306152T= | GRCh38 |
NC_000002.11:g.46533291T= , CM000664.1:g.46533291T= | GRCh37 |
NC_000002.10:g.46386795T= | NCBI36 |
NG_016000.1:g.13751T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263734.5:c.26+8215T= MANE Select | ENSP00000263734.3:n.26+8215T= | |
ENST00000263734.4:c.26+8215T= | ENSP00000263734.3:n.26+8215T= | |
ENST00000449347.5:c.26+8215T= | ENSP00000406137.1:n.26+8215T= | |
ENST00000460015.1:n.432+12054T= | ||
ENST00000467888.5:n.174+8215T= | ||
NM_001430.4:c.26+8215T= | NP_001421.2:n.26+8215T= | |
XR_940055.1:n.2501+7941A= | ||
NM_001430.5:c.26+8215T= MANE Select | NP_001421.2:n.26+8215T= |