Canonical Allele Identifier: CA2259200248
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057242789
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664906C>T , CM000679.2:g.39664906C>T GRCh38
NC_000017.10:g.37821159C>T , CM000679.1:g.37821159C>T GRCh37
NC_000017.9:g.35074685C>T NCBI36
NG_008892.1:g.4561C>T , LRG_210:g.4561C>T
NG_042278.1:g.1926C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-454C>T ENSP00000312624.2:n.-454C>T
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Search 100 bp 3'