HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133258102T>A , CM000671.2:g.133258102T>A | GRCh38 |
NC_000009.11:g.136133492T>A , CM000671.1:g.136133492T>A | GRCh37 |
NC_000009.10:g.135123313T>A | NCBI36 |
NG_006669.1:g.19562A>T | |
NG_006669.2:g.22113A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.264A>T | ||
ENST00000647353.1:n.54-6950A>T | ||
ENST00000651471.1:n.269A>T | ||
ENST00000679909.1:c.28+17060A>T | ENSP00000506089.1:n.28+17060A>T | |
ENST00000453660.3:n.246A>T | ||
ENST00000538324.2:c.234A>T | ENSP00000483018.1:p.Thr78= | |
ENST00000611156.4:c.234A>T | ENSP00000483265.1:p.Thr78= | |
NM_020469.2:c.234A>T | NP_065202.2:p.Thr78= | |
NM_020469.3:c.234A>T | NP_065202.2:p.Thr78= |