Canonical Allele Identifier: CA2259200281
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057243507
gnomAD v4: 17-39664982-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664982G>A , CM000679.2:g.39664982G>A GRCh38
NC_000017.10:g.37821235G>A , CM000679.1:g.37821235G>A GRCh37
NC_000017.9:g.35074761G>A NCBI36
NG_008892.1:g.4637G>A , LRG_210:g.4637G>A
NG_042278.1:g.2002G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-378G>A ENSP00000312624.2:n.-378G>A
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