Canonical Allele Identifier: CA129084985
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1033105432
gnomAD v4: 5-149981965-A-C
MyVariant Identifiers: chr5:g.149361528A>C (hg19) chr5:g.149981965A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981965A>C , CM000667.2:g.149981965A>C GRCh38
NC_000005.9:g.149361528A>C , CM000667.1:g.149361528A>C GRCh37
NC_000005.8:g.149341721A>C NCBI36
NG_007147.2:g.23083A>C , LRG_684:g.23083A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*152A>C MANE Select ENSP00000286298.4:n.*152A>C
ENST00000286298.4:c.*152A>C ENSP00000286298.4:n.*152A>C
ENST00000503336.1:c.372+3614A>C ENSP00000426053.1:n.372+3614A>C
NM_000112.3:c.*152A>C , LRG_684t1:c.*152A>C NP_000103.2:n.*152A>C
XM_017009191.2:c.*49A>C XP_016864680.1:n.*49A>C
NM_000112.4:c.*152A>C MANE Select NP_000103.2:n.*152A>C
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