Canonical Allele Identifier: CA2259200228
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664873C= , CM000679.2:g.39664873C= GRCh38
NC_000017.10:g.37821126C= , CM000679.1:g.37821126C= GRCh37
NC_000017.9:g.35074652C= NCBI36
NG_008892.1:g.4528C= , LRG_210:g.4528C=
NG_042278.1:g.1893C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-487C= ENSP00000312624.2:n.-487C=