Canonical Allele Identifier: CA2637632107
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665326G>A , CM000679.2:g.39665326G>A GRCh38
NC_000017.10:g.37821579G>A , CM000679.1:g.37821579G>A GRCh37
NC_000017.9:g.35075105G>A NCBI36
NG_008892.1:g.4981G>A , LRG_210:g.4981G>A
NG_042278.1:g.2346G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-34G>A ENSP00000312624.2:n.-34G>A