Canonical Allele Identifier: CA361705470
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs563310012
gnomAD v3: 5-149978313-G-T
gnomAD v4: 5-149978313-G-T
MyVariant Identifiers: chr5:g.149357876G>T (hg19) chr5:g.149978313G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149978313G>T , CM000667.2:g.149978313G>T GRCh38
NC_000005.9:g.149357876G>T , CM000667.1:g.149357876G>T GRCh37
NC_000005.8:g.149338069G>T NCBI36
NG_007147.2:g.19431G>T , LRG_684:g.19431G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000690410.1:n.893G>T
ENST00000286298.5:c.661G>T MANE Select ENSP00000286298.4:p.Val221Phe
ENST00000286298.4:c.661G>T ENSP00000286298.4:p.Val221Phe
ENST00000503336.1:c.334G>T ENSP00000426053.1:p.Val112Phe
NM_000112.3:c.661G>T , LRG_684t1:c.661G>T NP_000103.2:p.Val221Phe
XM_017009191.2:c.661G>T XP_016864680.1:p.Val221Phe
NM_000112.4:c.661G>T MANE Select NP_000103.2:p.Val221Phe
Search 100 bp 5'
Search 100 bp 3'