Canonical Allele Identifier: CA2637631392
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39664977-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664980del , CM000679.2:g.39664980del GRCh38
NC_000017.10:g.37821233del , CM000679.1:g.37821233del GRCh37
NC_000017.9:g.35074759del NCBI36
NG_008892.1:g.4635del , LRG_210:g.4635del
NG_042278.1:g.2000del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-380del ENSP00000312624.2:n.-380del
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