Canonical Allele Identifier: CA290433255
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1046923908
gnomAD v3: 17-39664895-C-T
gnomAD v4: 17-39664895-C-T
MyVariant Identifiers: chr17:g.37821148C>T (hg19) chr17:g.39664895C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664895C>T , CM000679.2:g.39664895C>T GRCh38
NC_000017.10:g.37821148C>T , CM000679.1:g.37821148C>T GRCh37
NC_000017.9:g.35074674C>T NCBI36
NG_008892.1:g.4550C>T , LRG_210:g.4550C>T
NG_042278.1:g.1915C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-465C>T ENSP00000312624.2:n.-465C>T
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