Canonical Allele Identifier: CA275015096
Gene:

Linked Data

dbSNP Id: rs139368599
gnomAD v2: 15-87962712-C-T
gnomAD v3: 15-87419481-C-T
gnomAD v4: 15-87419481-C-T
MyVariant Identifiers: chr15:g.87962712C>T (hg19) chr15:g.87419481C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419481C>T , CM000677.2:g.87419481C>T GRCh38
NC_000015.9:g.87962712C>T , CM000677.1:g.87962712C>T GRCh37
NC_000015.8:g.85763716C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-210G>A
XR_932585.1:n.340-210G>A
XR_001751647.1:n.617-210G>A
XR_932585.2:n.627-210G>A
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