Canonical Allele Identifier: CA983629061
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs768159521

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665303G>A , CM000679.2:g.39665303G>A GRCh38
NC_000017.10:g.37821556G>A , CM000679.1:g.37821556G>A GRCh37
NC_000017.9:g.35075082G>A NCBI36
NG_008892.1:g.4958G>A , LRG_210:g.4958G>A
NG_042278.1:g.2323G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-57G>A ENSP00000312624.2:n.-57G>A