Canonical Allele Identifier: CA368851385
Gene: SLC26A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107420144C>T (hg19) chr7:g.107779699C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779699C>T , CM000669.2:g.107779699C>T GRCh38
NC_000007.13:g.107420144C>T , CM000669.1:g.107420144C>T GRCh37
NC_000007.12:g.107207380C>T NCBI36
NG_008046.1:g.28535G>A , LRG_683:g.28535G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1376G>A MANE Select ENSP00000345873.5:p.Gly459Asp
ENST00000340010.9:c.1376G>A ENSP00000345873.5:p.Gly459Asp
ENST00000379083.7:c.*1167G>A ENSP00000368375.3:n.*1167G>A
NM_000111.2:c.1376G>A , LRG_683t1:c.1376G>A NP_000102.1:p.Gly459Asp
XM_011515867.1:c.1376G>A XP_011514169.1:p.Gly459Asp
NM_000111.3:c.1376G>A MANE Select NP_000102.1:p.Gly459Asp
Search 100 bp 5'
Search 100 bp 3'