Canonical Allele Identifier: CA2637632124
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665345G>A , CM000679.2:g.39665345G>A GRCh38
NC_000017.10:g.37821598G>A , CM000679.1:g.37821598G>A GRCh37
NC_000017.9:g.35075124G>A NCBI36
NG_008892.1:g.5000G>A , LRG_210:g.5000G>A
NG_042278.1:g.2365G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-15G>A ENSP00000312624.2:n.-15G>A