Canonical Allele Identifier: CA361705193

Gene: SLC26A2

Linked Data

• MyVariant Identifiers: chr5:g.149357751A>G (hg19) ; chr5:g.149978188A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149978188A>G , CM000667.2:g.149978188A>G	GRCh38
NC_000005.9:g.149357751A>G , CM000667.1:g.149357751A>G	GRCh37
NC_000005.8:g.149337944A>G	NCBI36
NG_007147.2:g.19306A>G , LRG_684:g.19306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000690410.1:n.768A>G
ENST00000286298.5:c.536A>G MANE Select	ENSP00000286298.4:p.Glu179Gly
ENST00000286298.4:c.536A>G	ENSP00000286298.4:p.Glu179Gly
ENST00000503336.1:c.209A>G	ENSP00000426053.1:p.Glu70Gly
NM_000112.3:c.536A>G , LRG_684t1:c.536A>G	NP_000103.2:p.Glu179Gly
XM_017009191.2:c.536A>G	XP_016864680.1:p.Glu179Gly
NM_000112.4:c.536A>G MANE Select	NP_000103.2:p.Glu179Gly