Canonical Allele Identifier: CA2637632111
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665328G>C , CM000679.2:g.39665328G>C GRCh38
NC_000017.10:g.37821581G>C , CM000679.1:g.37821581G>C GRCh37
NC_000017.9:g.35075107G>C NCBI36
NG_008892.1:g.4983G>C , LRG_210:g.4983G>C
NG_042278.1:g.2348G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-32G>C ENSP00000312624.2:n.-32G>C