Canonical Allele Identifier: CA983629009
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057245775

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665257C>T , CM000679.2:g.39665257C>T GRCh38
NC_000017.10:g.37821510C>T , CM000679.1:g.37821510C>T GRCh37
NC_000017.9:g.35075036C>T NCBI36
NG_008892.1:g.4912C>T , LRG_210:g.4912C>T
NG_042278.1:g.2277C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-103C>T ENSP00000312624.2:n.-103C>T