Canonical Allele Identifier: CA2733572967
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145071848

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665334del , CM000679.2:g.39665334del GRCh38
NC_000017.10:g.37821587del , CM000679.1:g.37821587del GRCh37
NC_000017.9:g.35075113del NCBI36
NG_008892.1:g.4989del , LRG_210:g.4989del
NG_042278.1:g.2354del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-26del ENSP00000312624.2:n.-26del