Canonical Allele Identifier: CA275015093
Gene:

Linked Data

dbSNP Id: rs1004586465
gnomAD v3: 15-87419462-C-G
gnomAD v4: 15-87419462-C-G
MyVariant Identifiers: chr15:g.87962693C>G (hg19) chr15:g.87419462C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419462C>G , CM000677.2:g.87419462C>G GRCh38
NC_000015.9:g.87962693C>G , CM000677.1:g.87962693C>G GRCh37
NC_000015.8:g.85763697C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-191G>C
XR_932585.1:n.340-191G>C
XR_001751647.1:n.617-191G>C
XR_932585.2:n.627-191G>C
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