HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133255888G>T , CM000671.2:g.133255888G>T | GRCh38 |
NC_000009.11:g.136131275G>T , CM000671.1:g.136131275G>T | GRCh37 |
NC_000009.10:g.135121096G>T | NCBI36 |
NG_006669.1:g.21780C>A | |
NG_006669.2:g.24328C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000453660.4:n.872C>A | ||
ENST00000647353.1:n.54-4736C>A | ||
ENST00000679909.1:c.28+19274C>A | ENSP00000506089.1:n.28+19274C>A | |
ENST00000453660.3:n.854C>A | ||
ENST00000538324.2:c.840C>A | ENSP00000483018.1:p.Thr280= | |
ENST00000611156.4:c.840C>A | ENSP00000483265.1:p.Thr280= | |
NM_020469.2:c.843C>A | NP_065202.2:p.Thr281= | |
NM_020469.3:c.843C>A | NP_065202.2:p.Thr281= |