Canonical Allele Identifier: CA308816

Gene: TCAP

Linked Data

• ClinVar Variation Id: 202101
• ClinVar RCV Id: RCV000183917 ; RCV002500551
• dbSNP Id: rs368175926
• ExAC: 17:37821600 A / G
• gnomAD v2: 17-37821600-A-G
• gnomAD v3: 17-39665347-A-G
• gnomAD v4: 17-39665347-A-G
• MyVariant Identifiers: chr17:g.37821600A>G (hg19) ; chr17:g.39665347A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665347A>G , CM000679.2:g.39665347A>G	GRCh38
NC_000017.10:g.37821600A>G , CM000679.1:g.37821600A>G	GRCh37
NC_000017.9:g.35075126A>G	NCBI36
NG_008892.1:g.5002A>G , LRG_210:g.5002A>G
NG_042278.1:g.2367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-13A>G	ENSP00000312624.2:n.-13A>G
NM_003673.3:c.-13A>G , LRG_210t1:c.-13A>G	NP_003664.1:n.-13A>G