Canonical Allele Identifier: CA2259200279
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664981A= , CM000679.2:g.39664981A= GRCh38
NC_000017.10:g.37821234A= , CM000679.1:g.37821234A= GRCh37
NC_000017.9:g.35074760A= NCBI36
NG_008892.1:g.4636A= , LRG_210:g.4636A=
NG_042278.1:g.2001A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-379A= ENSP00000312624.2:n.-379A=