Canonical Allele Identifier: CA2809442533
Gene: TCAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664862G>A , CM000679.2:g.39664862G>A GRCh38
NC_000017.10:g.37821115G>A , CM000679.1:g.37821115G>A GRCh37
NC_000017.9:g.35074641G>A NCBI36
NG_008892.1:g.4517G>A , LRG_210:g.4517G>A
NG_042278.1:g.1882G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-498G>A ENSP00000312624.2:n.-498G>A
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