HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133261643C>T , CM000671.2:g.133261643C>T | GRCh38 |
NC_000009.11:g.136137046C>T , CM000671.1:g.136137046C>T | GRCh37 |
NC_000009.10:g.135126867C>T | NCBI36 |
NG_006669.1:g.16007G>A | |
NG_006669.2:g.18572G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.129-269G>A | ||
ENST00000647353.1:n.54-10491G>A | ||
ENST00000651471.1:n.134-269G>A | ||
ENST00000679909.1:c.28+13519G>A | ENSP00000506089.1:n.28+13519G>A | |
ENST00000453660.3:n.111-269G>A | ||
ENST00000538324.2:c.99-269G>A | ENSP00000483018.1:n.99-269G>A | |
ENST00000611156.4:c.99-269G>A | ENSP00000483265.1:n.99-269G>A | |
NM_020469.2:c.99-269G>A | NP_065202.2:n.99-269G>A | |
NM_020469.3:c.99-269G>A | NP_065202.2:n.99-269G>A |