Canonical Allele Identifier: CA2637631977
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665236dup , CM000679.2:g.39665236dup GRCh38
NC_000017.10:g.37821489dup , CM000679.1:g.37821489dup GRCh37
NC_000017.9:g.35075015dup NCBI36
NG_008892.1:g.4891dup , LRG_210:g.4891dup
NG_042278.1:g.2256dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-124dup ENSP00000312624.2:n.-124dup