HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133260237T>C , CM000671.2:g.133260237T>C | GRCh38 |
NC_000009.11:g.136135641T>C , CM000671.1:g.136135641T>C | GRCh37 |
NC_000009.10:g.135125462T>C | NCBI36 |
NG_006669.1:g.17413A>G | |
NG_006669.2:g.19978A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.186-371A>G | ||
ENST00000647353.1:n.54-9085A>G | ||
ENST00000651471.1:n.191-371A>G | ||
ENST00000679909.1:c.28+14925A>G | ENSP00000506089.1:n.28+14925A>G | |
ENST00000453660.3:n.168-371A>G | ||
ENST00000538324.2:c.156-371A>G | ENSP00000483018.1:n.156-371A>G | |
ENST00000611156.4:c.156-371A>G | ENSP00000483265.1:n.156-371A>G | |
NM_020469.2:c.156-371A>G | NP_065202.2:n.156-371A>G | |
NM_020469.3:c.156-371A>G | NP_065202.2:n.156-371A>G |