Canonical Allele Identifier: CA361704762
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357543G>A (hg19) chr5:g.149977980G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977980G>A , CM000667.2:g.149977980G>A GRCh38
NC_000005.9:g.149357543G>A , CM000667.1:g.149357543G>A GRCh37
NC_000005.8:g.149337736G>A NCBI36
NG_007147.2:g.19098G>A , LRG_684:g.19098G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.560G>A
ENST00000286298.5:c.328G>A MANE Select ENSP00000286298.4:p.Gly110Arg
ENST00000286298.4:c.328G>A ENSP00000286298.4:p.Gly110Arg
ENST00000503336.1:c.1G>A ENSP00000426053.1:p.Gly1Arg
NM_000112.3:c.328G>A , LRG_684t1:c.328G>A NP_000103.2:p.Gly110Arg
XM_017009191.2:c.328G>A XP_016864680.1:p.Gly110Arg
NM_000112.4:c.328G>A MANE Select NP_000103.2:p.Gly110Arg
Search 100 bp 5'
Search 100 bp 3'