Canonical Allele Identifier: CA771857652
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1185321572
gnomAD v4: 17-39665067-G-A
MyVariant Identifiers: chr17:g.37821320G>A (hg19) chr17:g.39665067G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665067G>A , CM000679.2:g.39665067G>A GRCh38
NC_000017.10:g.37821320G>A , CM000679.1:g.37821320G>A GRCh37
NC_000017.9:g.35074846G>A NCBI36
NG_008892.1:g.4722G>A , LRG_210:g.4722G>A
NG_042278.1:g.2087G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-293G>A ENSP00000312624.2:n.-293G>A
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