Canonical Allele Identifier: CA2259200280
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664982G= , CM000679.2:g.39664982G= GRCh38
NC_000017.10:g.37821235G= , CM000679.1:g.37821235G= GRCh37
NC_000017.9:g.35074761G= NCBI36
NG_008892.1:g.4637G= , LRG_210:g.4637G=
NG_042278.1:g.2002G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-378G= ENSP00000312624.2:n.-378G=