Canonical Allele Identifier: CA2259200442
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665280G= , CM000679.2:g.39665280G= GRCh38
NC_000017.10:g.37821533G= , CM000679.1:g.37821533G= GRCh37
NC_000017.9:g.35075059G= NCBI36
NG_008892.1:g.4935G= , LRG_210:g.4935G=
NG_042278.1:g.2300G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-80G= ENSP00000312624.2:n.-80G=