Canonical Allele Identifier: CA625938786

Gene: TCAP

Linked Data

• dbSNP Id: rs1190054630
• gnomAD v2: 17-37821588-A-C
• gnomAD v4: 17-39665335-A-C
• MyVariant Identifiers: chr17:g.37821588A>C (hg19) ; chr17:g.39665335A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665335A>C , CM000679.2:g.39665335A>C	GRCh38
NC_000017.10:g.37821588A>C , CM000679.1:g.37821588A>C	GRCh37
NC_000017.9:g.35075114A>C	NCBI36
NG_008892.1:g.4990A>C , LRG_210:g.4990A>C
NG_042278.1:g.2355A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000309889.2:c.-25A>C	ENSP00000312624.2:n.-25A>C