Canonical Allele Identifier: CA2259200250
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057242806
gnomAD v4: 17-39664909-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664909G>A , CM000679.2:g.39664909G>A GRCh38
NC_000017.10:g.37821162G>A , CM000679.1:g.37821162G>A GRCh37
NC_000017.9:g.35074688G>A NCBI36
NG_008892.1:g.4564G>A , LRG_210:g.4564G>A
NG_042278.1:g.1929G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-451G>A ENSP00000312624.2:n.-451G>A
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