Canonical Allele Identifier: CA2259200262
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664945G= , CM000679.2:g.39664945G= GRCh38
NC_000017.10:g.37821198G= , CM000679.1:g.37821198G= GRCh37
NC_000017.9:g.35074724G= NCBI36
NG_008892.1:g.4600G= , LRG_210:g.4600G=
NG_042278.1:g.1965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-415G= ENSP00000312624.2:n.-415G=