Canonical Allele Identifier: CA361709929
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149361309T>G (hg19) chr5:g.149981746T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981746T>G , CM000667.2:g.149981746T>G GRCh38
NC_000005.9:g.149361309T>G , CM000667.1:g.149361309T>G GRCh37
NC_000005.8:g.149341502T>G NCBI36
NG_007147.2:g.22864T>G , LRG_684:g.22864T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.2153T>G MANE Select ENSP00000286298.4:p.Phe718Cys
ENST00000286298.4:c.2153T>G ENSP00000286298.4:p.Phe718Cys
ENST00000503336.1:c.372+3395T>G ENSP00000426053.1:n.372+3395T>G
NM_000112.3:c.2153T>G , LRG_684t1:c.2153T>G NP_000103.2:p.Phe718Cys
XM_017009191.2:c.2153T>G XP_016864680.1:p.Phe718Cys
NM_000112.4:c.2153T>G MANE Select NP_000103.2:p.Phe718Cys
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