Canonical Allele Identifier: CA368849496
Gene: SLC26A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767766C>G , CM000669.2:g.107767766C>G GRCh38
NC_000007.13:g.107408211C>G , CM000669.1:g.107408211C>G GRCh37
NC_000007.12:g.107195447C>G NCBI36
NG_008046.1:g.40468G>C , LRG_683:g.40468G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2205G>C MANE Select ENSP00000345873.5:p.Gln735His
ENST00000340010.9:c.2205G>C ENSP00000345873.5:p.Gln735His
ENST00000379083.7:c.*1762G>C ENSP00000368375.3:n.*1762G>C
NM_000111.2:c.2205G>C , LRG_683t1:c.2205G>C NP_000102.1:p.Gln735His
XM_011515867.1:c.2205G>C XP_011514169.1:p.Gln735His
NM_000111.3:c.2205G>C MANE Select NP_000102.1:p.Gln735His