HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133274161A>G , CM000671.2:g.133274161A>G | GRCh38 |
NC_000009.11:g.136149577A>G , CM000671.1:g.136149577A>G | GRCh37 |
NC_000009.10:g.135139398A>G | NCBI36 |
NG_006669.1:g.3474T>C | |
NG_006669.2:g.6054T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.58+1001T>C | ||
ENST00000647353.1:n.53+1001T>C | ||
ENST00000651471.1:n.63+1801T>C | ||
ENST00000679909.1:c.28+1001T>C | ENSP00000506089.1:n.28+1001T>C | |
ENST00000453660.3:n.40+1001T>C | ||
ENST00000538324.2:c.28+1001T>C | ENSP00000483018.1:n.28+1001T>C | |
ENST00000611156.4:c.28+1001T>C | ENSP00000483265.1:n.28+1001T>C | |
NM_020469.2:c.28+1001T>C | NP_065202.2:n.28+1001T>C | |
NM_020469.3:c.28+1001T>C | NP_065202.2:n.28+1001T>C |