HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256284G>A , CM000671.2:g.133256284G>A | GRCh38 |
NC_000009.11:g.136131671G>A , CM000671.1:g.136131671G>A | GRCh37 |
NC_000009.10:g.135121492G>A | NCBI36 |
NG_006669.1:g.21384C>T | |
NG_006669.2:g.23932C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.476C>T | ||
ENST00000647353.1:n.54-5132C>T | ||
ENST00000651471.1:n.402C>T | ||
ENST00000679909.1:c.28+18878C>T | ENSP00000506089.1:n.28+18878C>T | |
ENST00000453660.3:n.458C>T | ||
ENST00000538324.2:c.444C>T | ENSP00000483018.1:p.Tyr148= | |
ENST00000611156.4:c.444C>T | ENSP00000483265.1:p.Tyr148= | |
NM_020469.2:c.447C>T | NP_065202.2:p.Tyr149= | |
NM_020469.3:c.447C>T | NP_065202.2:p.Tyr149= |