Canonical Allele Identifier: CA290433340
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs115582106
gnomAD v2: 17-37821248-T-C
gnomAD v3: 17-39664995-T-C
gnomAD v4: 17-39664995-T-C
MyVariant Identifiers: chr17:g.37821248T>C (hg19) chr17:g.39664995T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664995T>C , CM000679.2:g.39664995T>C GRCh38
NC_000017.10:g.37821248T>C , CM000679.1:g.37821248T>C GRCh37
NC_000017.9:g.35074774T>C NCBI36
NG_008892.1:g.4650T>C , LRG_210:g.4650T>C
NG_042278.1:g.2015T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-365T>C ENSP00000312624.2:n.-365T>C
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