Canonical Allele Identifier: CA2809442537
Gene: TCAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664931C>T , CM000679.2:g.39664931C>T GRCh38
NC_000017.10:g.37821184C>T , CM000679.1:g.37821184C>T GRCh37
NC_000017.9:g.35074710C>T NCBI36
NG_008892.1:g.4586C>T , LRG_210:g.4586C>T
NG_042278.1:g.1951C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-429C>T ENSP00000312624.2:n.-429C>T
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