Canonical Allele Identifier: CA2259200488
Gene: TCAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665347A= , CM000679.2:g.39665347A= GRCh38
NC_000017.10:g.37821600A= , CM000679.1:g.37821600A= GRCh37
NC_000017.9:g.35075126A= NCBI36
NG_008892.1:g.5002A= , LRG_210:g.5002A=
NG_042278.1:g.2367A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-13A= ENSP00000312624.2:n.-13A=
NM_003673.3:c.-13A= , LRG_210t1:c.-13A= NP_003664.1:n.-13A=