Canonical Allele Identifier: CA2675943675
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149981839-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981839T>G , CM000667.2:g.149981839T>G GRCh38
NC_000005.9:g.149361402T>G , CM000667.1:g.149361402T>G GRCh37
NC_000005.8:g.149341595T>G NCBI36
NG_007147.2:g.22957T>G , LRG_684:g.22957T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*26T>G MANE Select ENSP00000286298.4:n.*26T>G
ENST00000286298.4:c.*26T>G ENSP00000286298.4:n.*26T>G
ENST00000503336.1:c.372+3488T>G ENSP00000426053.1:n.372+3488T>G
NM_000112.3:c.*26T>G , LRG_684t1:c.*26T>G NP_000103.2:n.*26T>G
XM_017009191.2:c.*12+14T>G XP_016864680.1:n.*12+14T>G
NM_000112.4:c.*26T>G MANE Select NP_000103.2:n.*26T>G
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