Canonical Allele Identifier: CA2578989472
Gene: SLC26A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767663A>T , CM000669.2:g.107767663A>T GRCh38
NC_000007.13:g.107408108A>T , CM000669.1:g.107408108A>T GRCh37
NC_000007.12:g.107195344A>T NCBI36
NG_008046.1:g.40571T>A , LRG_683:g.40571T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2206-19T>A MANE Select ENSP00000345873.5:n.2206-19T>A
ENST00000340010.9:c.2206-19T>A ENSP00000345873.5:n.2206-19T>A
ENST00000379083.7:c.*1763-19T>A ENSP00000368375.3:n.*1763-19T>A
NM_000111.2:c.2206-19T>A , LRG_683t1:c.2206-19T>A NP_000102.1:n.2206-19T>A
XM_011515867.1:c.2206-19T>A XP_011514169.1:n.2206-19T>A
NM_000111.3:c.2206-19T>A MANE Select NP_000102.1:n.2206-19T>A