HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44290979T= , CM000683.2:g.44290979T= | GRCh38 |
NC_000021.8:g.45710862T= , CM000683.1:g.45710862T= | GRCh37 |
NC_000021.7:g.44535290T= | NCBI36 |
NG_009556.1:g.10100T= , LRG_18:g.10100T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.880-116T= MANE Select | ENSP00000291582.5:n.880-116T= | |
ENST00000291582.5:c.880-116T= | ENSP00000291582.5:n.880-116T= | |
ENST00000337909.5:n.225T= | ||
ENST00000397994.8:n.225T= | ||
ENST00000527919.5:n.1613-119T= | ||
ENST00000530812.5:n.2630-119T= | ||
NM_000383.3:c.880-116T= | NP_000374.1:n.880-116T= | |
XM_011529551.1:c.880-119T= | XP_011527853.1:n.880-119T= | |
NM_000383.4:c.880-116T= MANE Select | NP_000374.1:n.880-116T= |