HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133261728A>C , CM000671.2:g.133261728A>C | GRCh38 |
NC_000009.11:g.136137131A>C , CM000671.1:g.136137131A>C | GRCh37 |
NC_000009.10:g.135126952A>C | NCBI36 |
NG_006669.1:g.15922T>G | |
NG_006669.2:g.18487T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.129-354T>G | ||
ENST00000647353.1:n.54-10576T>G | ||
ENST00000651471.1:n.134-354T>G | ||
ENST00000679909.1:c.28+13434T>G | ENSP00000506089.1:n.28+13434T>G | |
ENST00000453660.3:n.111-354T>G | ||
ENST00000538324.2:c.99-354T>G | ENSP00000483018.1:n.99-354T>G | |
ENST00000611156.4:c.99-354T>G | ENSP00000483265.1:n.99-354T>G | |
NM_020469.2:c.99-354T>G | NP_065202.2:n.99-354T>G | |
NM_020469.3:c.99-354T>G | NP_065202.2:n.99-354T>G |