Canonical Allele Identifier: CA308816
Gene: TCAP HGNC NCBI

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)
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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
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