Canonical Allele Identifier: CA2259200337
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057244244

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665082dup , CM000679.2:g.39665082dup GRCh38
NC_000017.10:g.37821335dup , CM000679.1:g.37821335dup GRCh37
NC_000017.9:g.35074861dup NCBI36
NG_008892.1:g.4737dup , LRG_210:g.4737dup
NG_042278.1:g.2102dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-278dup ENSP00000312624.2:n.-278dup