HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256137C>T , CM000671.2:g.133256137C>T | GRCh38 |
NC_000009.11:g.136131524C>T , CM000671.1:g.136131524C>T | GRCh37 |
NC_000009.10:g.135121345C>T | NCBI36 |
NG_006669.1:g.21531G>A | |
NG_006669.2:g.24079G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.623G>A | ||
ENST00000647353.1:n.54-4985G>A | ||
ENST00000651471.1:n.549G>A | ||
ENST00000679909.1:c.28+19025G>A | ENSP00000506089.1:n.28+19025G>A | |
ENST00000453660.3:n.605G>A | ||
ENST00000538324.2:c.591G>A | ENSP00000483018.1:p.Arg197= | |
ENST00000611156.4:c.591G>A | ENSP00000483265.1:p.Arg197= | |
NM_020469.2:c.594G>A | NP_065202.2:p.Arg198= | |
NM_020469.3:c.594G>A | NP_065202.2:p.Arg198= |