HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133257128C= , CM000671.2:g.133257128C= | GRCh38 |
NC_000009.11:g.136132515C= , CM000671.1:g.136132515C= | GRCh37 |
NC_000009.10:g.135122336C= | NCBI36 |
NG_006669.1:g.20540G= | |
NG_006669.2:g.23088G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.403+281G= | ||
ENST00000647353.1:n.54-5976G= | ||
ENST00000651471.1:n.330-772G= | ||
ENST00000679909.1:c.28+18034G= | ENSP00000506089.1:n.28+18034G= | |
ENST00000453660.3:n.385+281G= | ||
ENST00000538324.2:c.371+281G= | ENSP00000483018.1:n.371+281G= | |
ENST00000611156.4:c.371+281G= | ENSP00000483265.1:n.371+281G= | |
NM_020469.2:c.374+281G= | NP_065202.2:n.374+281G= | |
NM_020469.3:c.374+281G= | NP_065202.2:n.374+281G= |