Canonical Allele Identifier: CA625938787
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs754946182

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665336G>T , CM000679.2:g.39665336G>T GRCh38
NC_000017.10:g.37821589G>T , CM000679.1:g.37821589G>T GRCh37
NC_000017.9:g.35075115G>T NCBI36
NG_008892.1:g.4991G>T , LRG_210:g.4991G>T
NG_042278.1:g.2356G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-24G>T ENSP00000312624.2:n.-24G>T