Canonical Allele Identifier: CA361705126
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357720T>A (hg19) chr5:g.149978157T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978157T>A , CM000667.2:g.149978157T>A GRCh38
NC_000005.9:g.149357720T>A , CM000667.1:g.149357720T>A GRCh37
NC_000005.8:g.149337913T>A NCBI36
NG_007147.2:g.19275T>A , LRG_684:g.19275T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.737T>A
ENST00000286298.5:c.505T>A MANE Select ENSP00000286298.4:p.Cys169Ser
ENST00000286298.4:c.505T>A ENSP00000286298.4:p.Cys169Ser
ENST00000503336.1:c.178T>A ENSP00000426053.1:p.Cys60Ser
NM_000112.3:c.505T>A , LRG_684t1:c.505T>A NP_000103.2:p.Cys169Ser
XM_017009191.2:c.505T>A XP_016864680.1:p.Cys169Ser
NM_000112.4:c.505T>A MANE Select NP_000103.2:p.Cys169Ser
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