Canonical Allele Identifier: CA290433580

Gene: TCAP

Linked Data

• dbSNP Id: rs1016346069
• gnomAD v3: 17-39665293-C-A
• gnomAD v4: 17-39665293-C-A
• MyVariant Identifiers: chr17:g.37821546C>A (hg19) ; chr17:g.39665293C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665293C>A , CM000679.2:g.39665293C>A	GRCh38
NC_000017.10:g.37821546C>A , CM000679.1:g.37821546C>A	GRCh37
NC_000017.9:g.35075072C>A	NCBI36
NG_008892.1:g.4948C>A , LRG_210:g.4948C>A
NG_042278.1:g.2313C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-67C>A	ENSP00000312624.2:n.-67C>A