Canonical Allele Identifier: CA2259200469
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665322T= , CM000679.2:g.39665322T= GRCh38
NC_000017.10:g.37821575T= , CM000679.1:g.37821575T= GRCh37
NC_000017.9:g.35075101T= NCBI36
NG_008892.1:g.4977T= , LRG_210:g.4977T=
NG_042278.1:g.2342T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-38T= ENSP00000312624.2:n.-38T=