Canonical Allele Identifier: CA619736711
Gene:

Linked Data

dbSNP Id: rs1433087275
gnomAD v2: 15-87962699-G-C
gnomAD v3: 15-87419468-G-C
gnomAD v4: 15-87419468-G-C
MyVariant Identifiers: chr15:g.87962699G>C (hg19) chr15:g.87419468G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419468G>C , CM000677.2:g.87419468G>C GRCh38
NC_000015.9:g.87962699G>C , CM000677.1:g.87962699G>C GRCh37
NC_000015.8:g.85763703G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-197C>G
XR_932585.1:n.340-197C>G
XR_001751647.1:n.617-197C>G
XR_932585.2:n.627-197C>G
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