Canonical Allele Identifier: CA2259200431
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665261T= , CM000679.2:g.39665261T= GRCh38
NC_000017.10:g.37821514T= , CM000679.1:g.37821514T= GRCh37
NC_000017.9:g.35075040T= NCBI36
NG_008892.1:g.4916T= , LRG_210:g.4916T=
NG_042278.1:g.2281T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-99T= ENSP00000312624.2:n.-99T=