Canonical Allele Identifier: CA8532811
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs777779763

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665337G>A , CM000679.2:g.39665337G>A GRCh38
NC_000017.10:g.37821590G>A , CM000679.1:g.37821590G>A GRCh37
NC_000017.9:g.35075116G>A NCBI36
NG_008892.1:g.4992G>A , LRG_210:g.4992G>A
NG_042278.1:g.2357G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-23G>A ENSP00000312624.2:n.-23G>A