Canonical Allele Identifier: CA2259200424
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665239T= , CM000679.2:g.39665239T= GRCh38
NC_000017.10:g.37821492T= , CM000679.1:g.37821492T= GRCh37
NC_000017.9:g.35075018T= NCBI36
NG_008892.1:g.4894T= , LRG_210:g.4894T=
NG_042278.1:g.2259T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-121T= ENSP00000312624.2:n.-121T=