Canonical Allele Identifier: CA275015095
Gene:

Linked Data

dbSNP Id: rs867530722
gnomAD v2: 15-87962711-G-A
gnomAD v3: 15-87419480-G-A
gnomAD v4: 15-87419480-G-A
MyVariant Identifiers: chr15:g.87962711G>A (hg19) chr15:g.87419480G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419480G>A , CM000677.2:g.87419480G>A GRCh38
NC_000015.9:g.87962711G>A , CM000677.1:g.87962711G>A GRCh37
NC_000015.8:g.85763715G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-209C>T
XR_932585.1:n.340-209C>T
XR_001751647.1:n.617-209C>T
XR_932585.2:n.627-209C>T
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