Canonical Allele Identifier: CA619736698
Gene:

Linked Data

dbSNP Id: rs1427418178
gnomAD v2: 15-87962662-G-C
gnomAD v3: 15-87419431-G-C
gnomAD v4: 15-87419431-G-C
MyVariant Identifiers: chr15:g.87962662G>C (hg19) chr15:g.87419431G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419431G>C , CM000677.2:g.87419431G>C GRCh38
NC_000015.9:g.87962662G>C , CM000677.1:g.87962662G>C GRCh37
NC_000015.8:g.85763666G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932584.1:n.340-160C>G
XR_932585.1:n.340-160C>G
XR_001751647.1:n.617-160C>G
XR_932585.2:n.627-160C>G
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