Canonical Allele Identifier: CA2636607015

Gene: SLC47A2

Linked Data

• gnomAD v4: 17-19716692-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19716692A>T , CM000679.2:g.19716692A>T	GRCh38
NC_000017.10:g.19620005A>T , CM000679.1:g.19620005A>T	GRCh37
NC_000017.9:g.19560597A>T	NCBI36
NG_052805.1:g.7288T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350657.9:c.-137T>A	ENSP00000338084.6:n.-137T>A
ENST00000433844.2:c.-137T>A	ENSP00000391848.2:n.-137T>A
ENST00000456947.3:n.2146T>A
ENST00000463318.5:n.869+1419T>A
ENST00000467379.1:n.752T>A
NM_001099646.1:c.-137T>A	NP_001093116.1:n.-137T>A
NM_001256663.1:c.-137T>A	NP_001243592.1:n.-137T>A
NM_152908.3:c.-137T>A	NP_690872.2:n.-137T>A
XM_011523672.1:c.82-1475T>A	XP_011521974.1:n.82-1475T>A
XM_011523673.1:c.-25+770T>A	XP_011521975.1:n.-25+770T>A
XM_011523674.1:c.-25+770T>A	XP_011521976.1:n.-25+770T>A
XR_243543.3:n.732+1419T>A
NR_135624.1:n.869+1419T>A
NR_135625.1:n.39T>A
XM_017024222.2:c.-25+1419T>A	XP_016879711.1:n.-25+1419T>A
NR_135624.2:n.869+1419T>A