Canonical Allele Identifier: CA2259200436
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057245888

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665268T>A , CM000679.2:g.39665268T>A GRCh38
NC_000017.10:g.37821521T>A , CM000679.1:g.37821521T>A GRCh37
NC_000017.9:g.35075047T>A NCBI36
NG_008892.1:g.4923T>A , LRG_210:g.4923T>A
NG_042278.1:g.2288T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-92T>A ENSP00000312624.2:n.-92T>A