HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133257296G>T , CM000671.2:g.133257296G>T | GRCh38 |
NC_000009.11:g.136132683G>T , CM000671.1:g.136132683G>T | GRCh37 |
NC_000009.10:g.135122504G>T | NCBI36 |
NG_006669.1:g.20372C>A | |
NG_006669.2:g.22920C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.403+113C>A | ||
ENST00000647353.1:n.54-6144C>A | ||
ENST00000651471.1:n.329+746C>A | ||
ENST00000679909.1:c.28+17866C>A | ENSP00000506089.1:n.28+17866C>A | |
ENST00000453660.3:n.385+113C>A | ||
ENST00000538324.2:c.371+113C>A | ENSP00000483018.1:n.371+113C>A | |
ENST00000611156.4:c.371+113C>A | ENSP00000483265.1:n.371+113C>A | |
NM_020469.2:c.374+113C>A | NP_065202.2:n.374+113C>A | |
NM_020469.3:c.374+113C>A | NP_065202.2:n.374+113C>A |