Canonical Allele Identifier: CA656366998
Gene: TCAP HGNC NCBI

Linked Data

COSMIC: COSN1718878 COSN1718879 COSN1718880
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665269G>A , CM000679.2:g.39665269G>A GRCh38
NC_000017.10:g.37821522G>A , CM000679.1:g.37821522G>A GRCh37
NC_000017.9:g.35075048G>A NCBI36
NG_008892.1:g.4924G>A , LRG_210:g.4924G>A
NG_042278.1:g.2289G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-91G>A ENSP00000312624.2:n.-91G>A
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