Canonical Allele Identifier: CA2259200231
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664877C= , CM000679.2:g.39664877C= GRCh38
NC_000017.10:g.37821130C= , CM000679.1:g.37821130C= GRCh37
NC_000017.9:g.35074656C= NCBI36
NG_008892.1:g.4532C= , LRG_210:g.4532C=
NG_042278.1:g.1897C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-483C= ENSP00000312624.2:n.-483C=