Canonical Allele Identifier: CA447402035
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357716A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978153A>G , CM000667.2:g.149978153A>G GRCh38
NC_000005.9:g.149357716A>G , CM000667.1:g.149357716A>G GRCh37
NC_000005.8:g.149337909A>G NCBI36
NG_007147.2:g.19271A>G , LRG_684:g.19271A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.733A>G
ENST00000286298.5:c.501A>G MANE Select ENSP00000286298.4:p.Val167=
ENST00000286298.4:c.501A>G ENSP00000286298.4:p.Val167=
ENST00000503336.1:c.174A>G ENSP00000426053.1:p.Val58=
NM_000112.3:c.501A>G , LRG_684t1:c.501A>G NP_000103.2:p.Val167=
XM_017009191.2:c.501A>G XP_016864680.1:p.Val167=
NM_000112.4:c.501A>G MANE Select NP_000103.2:p.Val167=
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