Canonical Allele Identifier: CA2637632112
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665329C>A , CM000679.2:g.39665329C>A GRCh38
NC_000017.10:g.37821582C>A , CM000679.1:g.37821582C>A GRCh37
NC_000017.9:g.35075108C>A NCBI36
NG_008892.1:g.4984C>A , LRG_210:g.4984C>A
NG_042278.1:g.2349C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-31C>A ENSP00000312624.2:n.-31C>A