Canonical Allele Identifier: CA2259200478
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665338G= , CM000679.2:g.39665338G= GRCh38
NC_000017.10:g.37821591G= , CM000679.1:g.37821591G= GRCh37
NC_000017.9:g.35075117G= NCBI36
NG_008892.1:g.4993G= , LRG_210:g.4993G=
NG_042278.1:g.2358G=

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.2:c.-22G= ENSP00000312624.2:n.-22G=