Canonical Allele Identifier: CA2259200331
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665074C= , CM000679.2:g.39665074C= GRCh38
NC_000017.10:g.37821327C= , CM000679.1:g.37821327C= GRCh37
NC_000017.9:g.35074853C= NCBI36
NG_008892.1:g.4729C= , LRG_210:g.4729C=
NG_042278.1:g.2094C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-286C= ENSP00000312624.2:n.-286C=