Canonical Allele Identifier: CA290433362
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1283322
ClinVar RCV Id: RCV001696466
dbSNP Id: rs35821333
gnomAD v2: 17-37821275-A-G
gnomAD v3: 17-39665022-A-G
gnomAD v4: 17-39665022-A-G
MyVariant Identifiers: chr17:g.37821275A>G (hg19) chr17:g.39665022A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665022A>G , CM000679.2:g.39665022A>G GRCh38
NC_000017.10:g.37821275A>G , CM000679.1:g.37821275A>G GRCh37
NC_000017.9:g.35074801A>G NCBI36
NG_008892.1:g.4677A>G , LRG_210:g.4677A>G
NG_042278.1:g.2042A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-338A>G ENSP00000312624.2:n.-338A>G
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