Canonical Allele Identifier: CA2251175718

Gene: SLC47A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19716685G= , CM000679.2:g.19716685G=	GRCh38
NC_000017.10:g.19619998G= , CM000679.1:g.19619998G=	GRCh37
NC_000017.9:g.19560590G=	NCBI36
NG_052805.1:g.7295C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001099646.1:c.-130C=	NP_001093116.1:n.-130C=
NM_001256663.1:c.-130C=	NP_001243592.1:n.-130C=
NM_152908.3:c.-130C=	NP_690872.2:n.-130C=
NR_135624.1:n.869+1426C=
NR_135624.2:n.869+1426C=
NR_135625.1:n.46C=
ENST00000350657.9:c.-130C=	ENSP00000338084.6:n.-130C=
ENST00000433844.2:c.-130C=	ENSP00000391848.2:n.-130C=
ENST00000456947.3:n.2153C=
ENST00000463318.5:n.869+1426C=
ENST00000467379.1:n.759C=
XM_011523672.1:c.82-1468C=	XP_011521974.1:n.82-1468C=
XM_011523673.1:c.-25+777C=	XP_011521975.1:n.-25+777C=
XM_011523674.1:c.-25+777C=	XP_011521976.1:n.-25+777C=
XM_017024222.2:c.-25+1426C=	XP_016879711.1:n.-25+1426C=
XR_243543.3:n.732+1426C=