Canonical Allele Identifier: CA290433260
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs922019691
MyVariant Identifiers: chr17:g.37821152C>G (hg19) chr17:g.39664899C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664899C>G , CM000679.2:g.39664899C>G GRCh38
NC_000017.10:g.37821152C>G , CM000679.1:g.37821152C>G GRCh37
NC_000017.9:g.35074678C>G NCBI36
NG_008892.1:g.4554C>G , LRG_210:g.4554C>G
NG_042278.1:g.1919C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-461C>G ENSP00000312624.2:n.-461C>G
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