Canonical Allele Identifier: CA2298481197
Gene:

Linked Data

dbSNP Id: rs1910117452
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477591T>A , CM000680.2:g.41477591T>A GRCh38
NC_000018.9:g.39057555T>A , CM000680.1:g.39057555T>A GRCh37
NC_000018.8:g.37311553T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26543T>A
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Search 100 bp 3'