Canonical Allele Identifier: CA457107553
Gene: SLC26A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107420131T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779686T>G , CM000669.2:g.107779686T>G GRCh38
NC_000007.13:g.107420131T>G , CM000669.1:g.107420131T>G GRCh37
NC_000007.12:g.107207367T>G NCBI36
NG_008046.1:g.28548A>C , LRG_683:g.28548A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340010.10:c.1389A>C MANE Select ENSP00000345873.5:p.Arg463=
ENST00000340010.9:c.1389A>C ENSP00000345873.5:p.Arg463=
ENST00000379083.7:c.*1180A>C ENSP00000368375.3:n.*1180A>C
NM_000111.2:c.1389A>C , LRG_683t1:c.1389A>C NP_000102.1:p.Arg463=
XM_011515867.1:c.1389A>C XP_011514169.1:p.Arg463=
NM_000111.3:c.1389A>C MANE Select NP_000102.1:p.Arg463=
Search 100 bp 5'
Search 100 bp 3'