Canonical Allele Identifier: CA2809442534
Gene: TCAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664875G>T , CM000679.2:g.39664875G>T GRCh38
NC_000017.10:g.37821128G>T , CM000679.1:g.37821128G>T GRCh37
NC_000017.9:g.35074654G>T NCBI36
NG_008892.1:g.4530G>T , LRG_210:g.4530G>T
NG_042278.1:g.1895G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-485G>T ENSP00000312624.2:n.-485G>T
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