Canonical Allele Identifier: CA2259200264
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057243183
gnomAD v4: 17-39664947-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664947C>A , CM000679.2:g.39664947C>A GRCh38
NC_000017.10:g.37821200C>A , CM000679.1:g.37821200C>A GRCh37
NC_000017.9:g.35074726C>A NCBI36
NG_008892.1:g.4602C>A , LRG_210:g.4602C>A
NG_042278.1:g.1967C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-413C>A ENSP00000312624.2:n.-413C>A
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