Canonical Allele Identifier: CA457205849
Gene: SLC26A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107408214A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107767769A>G , CM000669.2:g.107767769A>G GRCh38
NC_000007.13:g.107408214A>G , CM000669.1:g.107408214A>G GRCh37
NC_000007.12:g.107195450A>G NCBI36
NG_008046.1:g.40465T>C , LRG_683:g.40465T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.2202T>C MANE Select ENSP00000345873.5:p.Ser734=
ENST00000340010.9:c.2202T>C ENSP00000345873.5:p.Ser734=
ENST00000379083.7:c.*1759T>C ENSP00000368375.3:n.*1759T>C
NM_000111.2:c.2202T>C , LRG_683t1:c.2202T>C NP_000102.1:p.Ser734=
XM_011515867.1:c.2202T>C XP_011514169.1:p.Ser734=
NM_000111.3:c.2202T>C MANE Select NP_000102.1:p.Ser734=