Canonical Allele Identifier: CA2251175726

Gene: SLC47A2

Linked Data

• dbSNP Id: rs2086279056
• gnomAD v4: 17-19716700-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.19716700T>C , CM000679.2:g.19716700T>C	GRCh38
NC_000017.10:g.19620013T>C , CM000679.1:g.19620013T>C	GRCh37
NC_000017.9:g.19560605T>C	NCBI36
NG_052805.1:g.7280A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350657.9:c.-145A>G	ENSP00000338084.6:n.-145A>G
ENST00000433844.2:c.-145A>G	ENSP00000391848.2:n.-145A>G
ENST00000456947.3:n.2138A>G
ENST00000463318.5:n.869+1411A>G
ENST00000467379.1:n.744A>G
NM_001099646.1:c.-145A>G	NP_001093116.1:n.-145A>G
NM_001256663.1:c.-145A>G	NP_001243592.1:n.-145A>G
NM_152908.3:c.-145A>G	NP_690872.2:n.-145A>G
XM_011523672.1:c.82-1483A>G	XP_011521974.1:n.82-1483A>G
XM_011523673.1:c.-25+762A>G	XP_011521975.1:n.-25+762A>G
XM_011523674.1:c.-25+762A>G	XP_011521976.1:n.-25+762A>G
XR_243543.3:n.732+1411A>G
NR_135624.1:n.869+1411A>G
NR_135625.1:n.31A>G
XM_017024222.2:c.-25+1411A>G	XP_016879711.1:n.-25+1411A>G
NR_135624.2:n.869+1411A>G