HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44296276A>T , CM000683.2:g.44296276A>T | GRCh38 |
NC_000021.8:g.45716159A>T , CM000683.1:g.45716159A>T | GRCh37 |
NC_000021.7:g.44540587A>T | NCBI36 |
NG_009556.1:g.15397A>T , LRG_18:g.15397A>T | |
NG_034033.1:g.1243A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000291582.6:c.1504-107A>T MANE Select | ENSP00000291582.5:n.1504-107A>T | |
ENST00000291582.5:c.1504-107A>T | ENSP00000291582.5:n.1504-107A>T | |
ENST00000337909.5:n.965-107A>T | ||
ENST00000397994.8:n.883-107A>T | ||
ENST00000527919.5:n.2263-107A>T | ||
ENST00000530812.5:n.3251-107A>T | ||
NM_000383.3:c.1504-107A>T | NP_000374.1:n.1504-107A>T | |
XM_011529551.1:c.1501-107A>T | XP_011527853.1:n.1501-107A>T | |
NM_000383.4:c.1504-107A>T MANE Select | NP_000374.1:n.1504-107A>T |