HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255665C>T , CM000671.2:g.133255665C>T | GRCh38 |
NC_000009.11:g.136131052C>T , CM000671.1:g.136131052C>T | GRCh37 |
NC_000009.10:g.135120873C>T | NCBI36 |
NG_006669.1:g.22003G>A | |
NG_006669.2:g.24551G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.1095G>A | ||
ENST00000647353.1:n.54-4513G>A | ||
ENST00000679909.1:c.28+19497G>A | ENSP00000506089.1:n.28+19497G>A | |
ENST00000453660.3:n.1077G>A | ||
ENST00000538324.2:c.1059G>A | ENSP00000483018.1:p.Glu353= | |
ENST00000611156.4:c.*1G>A | ENSP00000483265.1:n.*1G>A | |
NM_020469.2:c.*1G>A | NP_065202.2:n.*1G>A | |
NM_020469.3:c.*1G>A | NP_065202.2:n.*1G>A |