Canonical Allele Identifier: CA2637631494
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665044A>C , CM000679.2:g.39665044A>C GRCh38
NC_000017.10:g.37821297A>C , CM000679.1:g.37821297A>C GRCh37
NC_000017.9:g.35074823A>C NCBI36
NG_008892.1:g.4699A>C , LRG_210:g.4699A>C
NG_042278.1:g.2064A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-316A>C ENSP00000312624.2:n.-316A>C