Canonical Allele Identifier: CA1082859046
Gene: SLC26A2 HGNC NCBI

Linked Data

dbSNP Id: rs1431423838
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981932T>C , CM000667.2:g.149981932T>C GRCh38
NC_000005.9:g.149361495T>C , CM000667.1:g.149361495T>C GRCh37
NC_000005.8:g.149341688T>C NCBI36
NG_007147.2:g.23050T>C , LRG_684:g.23050T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*119T>C MANE Select ENSP00000286298.4:n.*119T>C
ENST00000286298.4:c.*119T>C ENSP00000286298.4:n.*119T>C
ENST00000503336.1:c.372+3581T>C ENSP00000426053.1:n.372+3581T>C
NM_000112.3:c.*119T>C , LRG_684t1:c.*119T>C NP_000103.2:n.*119T>C
XM_017009191.2:c.*16T>C XP_016864680.1:n.*16T>C
NM_000112.4:c.*119T>C MANE Select NP_000103.2:n.*119T>C
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