Canonical Allele Identifier: CA361705111

Gene: SLC26A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978148G>C , CM000667.2:g.149978148G>C	GRCh38
NC_000005.9:g.149357711G>C , CM000667.1:g.149357711G>C	GRCh37
NC_000005.8:g.149337904G>C	NCBI36
NG_007147.2:g.19266G>C , LRG_684:g.19266G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000112.4:c.496G>C MANE Select	NP_000103.2:p.Gly166Arg
ENST00000286298.5:c.496G>C MANE Select	ENSP00000286298.4:p.Gly166Arg
NM_000112.3:c.496G>C , LRG_684t1:c.496G>C	NP_000103.2:p.Gly166Arg
ENST00000286298.4:c.496G>C	ENSP00000286298.4:p.Gly166Arg
ENST00000503336.1:c.169G>C	ENSP00000426053.1:p.Gly57Arg
ENST00000690410.1:n.728G>C
XM_017009191.2:c.496G>C	XP_016864680.1:p.Gly166Arg