HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255403T>A , CM000671.2:g.133255403T>A | GRCh38 |
NC_000009.11:g.136130790T>A , CM000671.1:g.136130790T>A | GRCh37 |
NC_000009.10:g.135120611T>A | NCBI36 |
NG_006669.1:g.22265A>T | |
NG_006669.2:g.24813A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.1357A>T | ||
ENST00000647353.1:n.54-4251A>T | ||
ENST00000679909.1:c.28+19759A>T | ENSP00000506089.1:n.28+19759A>T | |
ENST00000453660.3:n.1339A>T | ||
ENST00000611156.4:c.*263A>T | ENSP00000483265.1:n.*263A>T | |
NM_020469.2:c.*263A>T | NP_065202.2:n.*263A>T | |
NM_020469.3:c.*263A>T | NP_065202.2:n.*263A>T |