Canonical Allele Identifier: CA361704013
Gene: SLC26A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.149357325C>G (hg19) chr5:g.149977762C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149977762C>G , CM000667.2:g.149977762C>G GRCh38
NC_000005.9:g.149357325C>G , CM000667.1:g.149357325C>G GRCh37
NC_000005.8:g.149337518C>G NCBI36
NG_007147.2:g.18880C>G , LRG_684:g.18880C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000690410.1:n.342C>G
ENST00000286298.5:c.110C>G MANE Select ENSP00000286298.4:p.Thr37Ser
ENST00000286298.4:c.110C>G ENSP00000286298.4:p.Thr37Ser
NM_000112.3:c.110C>G , LRG_684t1:c.110C>G NP_000103.2:p.Thr37Ser
XM_017009191.2:c.110C>G XP_016864680.1:p.Thr37Ser
NM_000112.4:c.110C>G MANE Select NP_000103.2:p.Thr37Ser
Search 100 bp 5'
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