Canonical Allele Identifier: CA2259200261
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664941C= , CM000679.2:g.39664941C= GRCh38
NC_000017.10:g.37821194C= , CM000679.1:g.37821194C= GRCh37
NC_000017.9:g.35074720C= NCBI36
NG_008892.1:g.4596C= , LRG_210:g.4596C=
NG_042278.1:g.1961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-419C= ENSP00000312624.2:n.-419C=