Canonical Allele Identifier: CA2259200290
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664995T= , CM000679.2:g.39664995T= GRCh38
NC_000017.10:g.37821248T= , CM000679.1:g.37821248T= GRCh37
NC_000017.9:g.35074774T= NCBI36
NG_008892.1:g.4650T= , LRG_210:g.4650T=
NG_042278.1:g.2015T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-365T= ENSP00000312624.2:n.-365T=