Canonical Allele Identifier: CA2636607018

Gene: SLC47A2

Linked Data

• gnomAD v4: 17-19716694-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19716694G>T , CM000679.2:g.19716694G>T	GRCh38
NC_000017.10:g.19620007G>T , CM000679.1:g.19620007G>T	GRCh37
NC_000017.9:g.19560599G>T	NCBI36
NG_052805.1:g.7286C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350657.9:c.-139C>A	ENSP00000338084.6:n.-139C>A
ENST00000433844.2:c.-139C>A	ENSP00000391848.2:n.-139C>A
ENST00000456947.3:n.2144C>A
ENST00000463318.5:n.869+1417C>A
ENST00000467379.1:n.750C>A
NM_001099646.1:c.-139C>A	NP_001093116.1:n.-139C>A
NM_001256663.1:c.-139C>A	NP_001243592.1:n.-139C>A
NM_152908.3:c.-139C>A	NP_690872.2:n.-139C>A
XM_011523672.1:c.82-1477C>A	XP_011521974.1:n.82-1477C>A
XM_011523673.1:c.-25+768C>A	XP_011521975.1:n.-25+768C>A
XM_011523674.1:c.-25+768C>A	XP_011521976.1:n.-25+768C>A
XR_243543.3:n.732+1417C>A
NR_135624.1:n.869+1417C>A
NR_135625.1:n.37C>A
XM_017024222.2:c.-25+1417C>A	XP_016879711.1:n.-25+1417C>A
NR_135624.2:n.869+1417C>A