HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255705A>C , CM000671.2:g.133255705A>C | GRCh38 |
NC_000009.11:g.136131092A>C , CM000671.1:g.136131092A>C | GRCh37 |
NC_000009.10:g.135120913A>C | NCBI36 |
NG_006669.1:g.21963T>G | |
NG_006669.2:g.24511T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.1055T>G | ||
ENST00000647353.1:n.54-4553T>G | ||
ENST00000679909.1:c.28+19457T>G | ENSP00000506089.1:n.28+19457T>G | |
ENST00000453660.3:n.1037T>G | ||
ENST00000538324.2:c.1023T>G | ENSP00000483018.1:p.Thr341= | |
ENST00000611156.4:c.1023T>G | ENSP00000483265.1:p.Thr341= | |
NM_020469.2:c.1026T>G | NP_065202.2:p.Thr342= | |
NM_020469.3:c.1026T>G | NP_065202.2:p.Thr342= |