Canonical Allele Identifier: CA563955751
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1411372287
gnomAD v2: 5-149361410-A-T
gnomAD v4: 5-149981847-A-T
MyVariant Identifiers: chr5:g.149361410A>T (hg19) chr5:g.149981847A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981847A>T , CM000667.2:g.149981847A>T GRCh38
NC_000005.9:g.149361410A>T , CM000667.1:g.149361410A>T GRCh37
NC_000005.8:g.149341603A>T NCBI36
NG_007147.2:g.22965A>T , LRG_684:g.22965A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*34A>T MANE Select ENSP00000286298.4:n.*34A>T
ENST00000286298.4:c.*34A>T ENSP00000286298.4:n.*34A>T
ENST00000503336.1:c.372+3496A>T ENSP00000426053.1:n.372+3496A>T
NM_000112.3:c.*34A>T , LRG_684t1:c.*34A>T NP_000103.2:n.*34A>T
XM_017009191.2:c.*12+22A>T XP_016864680.1:n.*12+22A>T
NM_000112.4:c.*34A>T MANE Select NP_000103.2:n.*34A>T
Search 100 bp 5'
Search 100 bp 3'