Canonical Allele Identifier: CA361705173
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357741G>A (hg19) chr5:g.149978178G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978178G>A , CM000667.2:g.149978178G>A GRCh38
NC_000005.9:g.149357741G>A , CM000667.1:g.149357741G>A GRCh37
NC_000005.8:g.149337934G>A NCBI36
NG_007147.2:g.19296G>A , LRG_684:g.19296G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.758G>A
ENST00000286298.5:c.526G>A MANE Select ENSP00000286298.4:p.Val176Ile
ENST00000286298.4:c.526G>A ENSP00000286298.4:p.Val176Ile
ENST00000503336.1:c.199G>A ENSP00000426053.1:p.Val67Ile
NM_000112.3:c.526G>A , LRG_684t1:c.526G>A NP_000103.2:p.Val176Ile
XM_017009191.2:c.526G>A XP_016864680.1:p.Val176Ile
NM_000112.4:c.526G>A MANE Select NP_000103.2:p.Val176Ile
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