Canonical Allele Identifier: CA2636607011

Gene: SLC47A2

Linked Data

• gnomAD v4: 17-19716691-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19716691C>A , CM000679.2:g.19716691C>A	GRCh38
NC_000017.10:g.19620004C>A , CM000679.1:g.19620004C>A	GRCh37
NC_000017.9:g.19560596C>A	NCBI36
NG_052805.1:g.7289G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350657.9:c.-136G>T	ENSP00000338084.6:n.-136G>T
ENST00000433844.2:c.-136G>T	ENSP00000391848.2:n.-136G>T
ENST00000456947.3:n.2147G>T
ENST00000463318.5:n.869+1420G>T
ENST00000467379.1:n.753G>T
NM_001099646.1:c.-136G>T	NP_001093116.1:n.-136G>T
NM_001256663.1:c.-136G>T	NP_001243592.1:n.-136G>T
NM_152908.3:c.-136G>T	NP_690872.2:n.-136G>T
XM_011523672.1:c.82-1474G>T	XP_011521974.1:n.82-1474G>T
XM_011523673.1:c.-25+771G>T	XP_011521975.1:n.-25+771G>T
XM_011523674.1:c.-25+771G>T	XP_011521976.1:n.-25+771G>T
XR_243543.3:n.732+1420G>T
NR_135624.1:n.869+1420G>T
NR_135625.1:n.40G>T
XM_017024222.2:c.-25+1420G>T	XP_016879711.1:n.-25+1420G>T
NR_135624.2:n.869+1420G>T