Canonical Allele Identifier: CA164238291
Gene: SLC26A3 HGNC NCBI

Linked Data

dbSNP Id: rs80191685
MyVariant Identifiers: chr7:g.107420041C>A (hg19) chr7:g.107779596C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107779596C>A , CM000669.2:g.107779596C>A GRCh38
NC_000007.13:g.107420041C>A , CM000669.1:g.107420041C>A GRCh37
NC_000007.12:g.107207277C>A NCBI36
NG_008046.1:g.28638G>T , LRG_683:g.28638G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340010.10:c.1407+72G>T MANE Select ENSP00000345873.5:n.1407+72G>T
ENST00000340010.9:c.1407+72G>T ENSP00000345873.5:n.1407+72G>T
ENST00000379083.7:c.*1198+72G>T ENSP00000368375.3:n.*1198+72G>T
NM_000111.2:c.1407+72G>T , LRG_683t1:c.1407+72G>T NP_000102.1:n.1407+72G>T
XM_011515867.1:c.1407+72G>T XP_011514169.1:n.1407+72G>T
NM_000111.3:c.1407+72G>T MANE Select NP_000102.1:n.1407+72G>T
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