Canonical Allele Identifier: CA2259200226
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664868T= , CM000679.2:g.39664868T= GRCh38
NC_000017.10:g.37821121T= , CM000679.1:g.37821121T= GRCh37
NC_000017.9:g.35074647T= NCBI36
NG_008892.1:g.4523T= , LRG_210:g.4523T=
NG_042278.1:g.1888T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-492T= ENSP00000312624.2:n.-492T=