Canonical Allele Identifier: CA2637631738
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665153del , CM000679.2:g.39665153del GRCh38
NC_000017.10:g.37821406del , CM000679.1:g.37821406del GRCh37
NC_000017.9:g.35074932del NCBI36
NG_008892.1:g.4808del , LRG_210:g.4808del
NG_042278.1:g.2173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-207del ENSP00000312624.2:n.-207del