Canonical Allele Identifier: CA290433369
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs917723505
gnomAD v4: 17-39665026-G-A
MyVariant Identifiers: chr17:g.37821279G>A (hg19) chr17:g.39665026G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665026G>A , CM000679.2:g.39665026G>A GRCh38
NC_000017.10:g.37821279G>A , CM000679.1:g.37821279G>A GRCh37
NC_000017.9:g.35074805G>A NCBI36
NG_008892.1:g.4681G>A , LRG_210:g.4681G>A
NG_042278.1:g.2046G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-334G>A ENSP00000312624.2:n.-334G>A
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