Canonical Allele Identifier: CA290433547

Gene: TCAP

Linked Data

• dbSNP Id: rs1028245252
• gnomAD v4: 17-39665280-G-A
• MyVariant Identifiers: chr17:g.37821533G>A (hg19) ; chr17:g.39665280G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665280G>A , CM000679.2:g.39665280G>A	GRCh38
NC_000017.10:g.37821533G>A , CM000679.1:g.37821533G>A	GRCh37
NC_000017.9:g.35075059G>A	NCBI36
NG_008892.1:g.4935G>A , LRG_210:g.4935G>A
NG_042278.1:g.2300G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-80G>A	ENSP00000312624.2:n.-80G>A