Canonical Allele Identifier: CA2259200220
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs17554665
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664852C>G , CM000679.2:g.39664852C>G GRCh38
NC_000017.10:g.37821105C>G , CM000679.1:g.37821105C>G GRCh37
NC_000017.9:g.35074631C>G NCBI36
NG_008892.1:g.4507C>G , LRG_210:g.4507C>G
NG_042278.1:g.1872C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-508C>G ENSP00000312624.2:n.-508C>G
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