Canonical Allele Identifier: CA368851366
Gene: SLC26A3 HGNC NCBI

Linked Data

gnomAD v4: 7-107779691-A-C
MyVariant Identifiers: chr7:g.107420136A>C (hg19) chr7:g.107779691A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779691A>C , CM000669.2:g.107779691A>C GRCh38
NC_000007.13:g.107420136A>C , CM000669.1:g.107420136A>C GRCh37
NC_000007.12:g.107207372A>C NCBI36
NG_008046.1:g.28543T>G , LRG_683:g.28543T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1384T>G MANE Select ENSP00000345873.5:p.Trp462Gly
ENST00000340010.9:c.1384T>G ENSP00000345873.5:p.Trp462Gly
ENST00000379083.7:c.*1175T>G ENSP00000368375.3:n.*1175T>G
NM_000111.2:c.1384T>G , LRG_683t1:c.1384T>G NP_000102.1:p.Trp462Gly
XM_011515867.1:c.1384T>G XP_011514169.1:p.Trp462Gly
NM_000111.3:c.1384T>G MANE Select NP_000102.1:p.Trp462Gly
Search 100 bp 5'
Search 100 bp 3'