Canonical Allele Identifier: CA290433561
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs45604543
gnomAD v4: 17-39665283-C-G
MyVariant Identifiers: chr17:g.37821536C>G (hg19) chr17:g.39665283C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665283C>G , CM000679.2:g.39665283C>G GRCh38
NC_000017.10:g.37821536C>G , CM000679.1:g.37821536C>G GRCh37
NC_000017.9:g.35075062C>G NCBI36
NG_008892.1:g.4938C>G , LRG_210:g.4938C>G
NG_042278.1:g.2303C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-77C>G ENSP00000312624.2:n.-77C>G
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