Canonical Allele Identifier: CA2259200357
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665123G= , CM000679.2:g.39665123G= GRCh38
NC_000017.10:g.37821376G= , CM000679.1:g.37821376G= GRCh37
NC_000017.9:g.35074902G= NCBI36
NG_008892.1:g.4778G= , LRG_210:g.4778G=
NG_042278.1:g.2143G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-237G= ENSP00000312624.2:n.-237G=