Canonical Allele Identifier: CA275015086
Gene:

Linked Data

dbSNP Id: rs181530599
gnomAD v3: 15-87419371-G-C
gnomAD v4: 15-87419371-G-C
MyVariant Identifiers: chr15:g.87962602G>C (hg19) chr15:g.87419371G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419371G>C , CM000677.2:g.87419371G>C GRCh38
NC_000015.9:g.87962602G>C , CM000677.1:g.87962602G>C GRCh37
NC_000015.8:g.85763606G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-100C>G
XR_932585.1:n.340-100C>G
XR_001751647.1:n.617-100C>G
XR_932585.2:n.627-100C>G
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