Canonical Allele Identifier: CA2259200299
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665017T= , CM000679.2:g.39665017T= GRCh38
NC_000017.10:g.37821270T= , CM000679.1:g.37821270T= GRCh37
NC_000017.9:g.35074796T= NCBI36
NG_008892.1:g.4672T= , LRG_210:g.4672T=
NG_042278.1:g.2037T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-343T= ENSP00000312624.2:n.-343T=