Canonical Allele Identifier: CA716729220
Gene:

Linked Data

dbSNP Id: rs1488427236
MyVariant Identifiers: chr15:g.87962515A>T (hg19) chr15:g.87419284A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419284A>T , CM000677.2:g.87419284A>T GRCh38
NC_000015.9:g.87962515A>T , CM000677.1:g.87962515A>T GRCh37
NC_000015.8:g.85763519A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-13T>A
XR_932585.1:n.340-13T>A
XR_001751647.1:n.617-13T>A
XR_932585.2:n.627-13T>A
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