HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133257059T= , CM000671.2:g.133257059T= | GRCh38 |
NC_000009.11:g.136132446T= , CM000671.1:g.136132446T= | GRCh37 |
NC_000009.10:g.135122267T= | NCBI36 |
NG_006669.1:g.20609A= | |
NG_006669.2:g.23157A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.403+350A= | ||
ENST00000647353.1:n.54-5907A= | ||
ENST00000651471.1:n.330-703A= | ||
ENST00000679909.1:c.28+18103A= | ENSP00000506089.1:n.28+18103A= | |
ENST00000453660.3:n.385+350A= | ||
ENST00000538324.2:c.371+350A= | ENSP00000483018.1:n.371+350A= | |
ENST00000611156.4:c.371+350A= | ENSP00000483265.1:n.371+350A= | |
NM_020469.2:c.374+350A= | NP_065202.2:n.374+350A= | |
NM_020469.3:c.374+350A= | NP_065202.2:n.374+350A= |