Canonical Allele Identifier: CA771857609
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1396268798
MyVariant Identifiers: chr17:g.37821190A>T (hg19) chr17:g.39664937A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664937A>T , CM000679.2:g.39664937A>T GRCh38
NC_000017.10:g.37821190A>T , CM000679.1:g.37821190A>T GRCh37
NC_000017.9:g.35074716A>T NCBI36
NG_008892.1:g.4592A>T , LRG_210:g.4592A>T
NG_042278.1:g.1957A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-423A>T ENSP00000312624.2:n.-423A>T
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