Canonical Allele Identifier: CA2259200456
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057246215

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665306G>A , CM000679.2:g.39665306G>A GRCh38
NC_000017.10:g.37821559G>A , CM000679.1:g.37821559G>A GRCh37
NC_000017.9:g.35075085G>A NCBI36
NG_008892.1:g.4961G>A , LRG_210:g.4961G>A
NG_042278.1:g.2326G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-54G>A ENSP00000312624.2:n.-54G>A