Canonical Allele Identifier: CA2637631979
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665236del , CM000679.2:g.39665236del GRCh38
NC_000017.10:g.37821489del , CM000679.1:g.37821489del GRCh37
NC_000017.9:g.35075015del NCBI36
NG_008892.1:g.4891del , LRG_210:g.4891del
NG_042278.1:g.2256del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-124del ENSP00000312624.2:n.-124del