Canonical Allele Identifier: CA1732790038
Gene: SLC26A3 HGNC NCBI

Linked Data

dbSNP Id: rs1775010074
gnomAD v4: 7-107767667-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767667A>G , CM000669.2:g.107767667A>G GRCh38
NC_000007.13:g.107408112A>G , CM000669.1:g.107408112A>G GRCh37
NC_000007.12:g.107195348A>G NCBI36
NG_008046.1:g.40567T>C , LRG_683:g.40567T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2206-23T>C MANE Select ENSP00000345873.5:n.2206-23T>C
ENST00000340010.9:c.2206-23T>C ENSP00000345873.5:n.2206-23T>C
ENST00000379083.7:c.*1763-23T>C ENSP00000368375.3:n.*1763-23T>C
NM_000111.2:c.2206-23T>C , LRG_683t1:c.2206-23T>C NP_000102.1:n.2206-23T>C
XM_011515867.1:c.2206-23T>C XP_011514169.1:n.2206-23T>C
NM_000111.3:c.2206-23T>C MANE Select NP_000102.1:n.2206-23T>C
Search 100 bp 5'
Search 100 bp 3'