HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129814196C= , CM000671.2:g.129814196C= | GRCh38 |
NC_000009.11:g.132576475C= , CM000671.1:g.132576475C= | GRCh37 |
NC_000009.10:g.131616296C= | NCBI36 |
NG_008049.1:g.14967G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351698.5:c.775G= MANE Select | ENSP00000345719.4:p.Asp259= | |
ENST00000651202.1:c.*43G= | ENSP00000498222.1:n.*43G= | |
ENST00000351698.4:c.775G= | ENSP00000345719.4:p.Asp259= | |
ENST00000474192.1:n.359G= | ||
NM_000113.2:c.775G= | NP_000104.1:p.Asp259= | |
XR_929731.1:n.1102G= | ||
XR_929731.3:n.970G= | ||
NM_000113.3:c.775G= MANE Select | NP_000104.1:p.Asp259= |