Canonical Allele Identifier: CA716729342
Gene:

Linked Data

dbSNP Id: rs1410263373
gnomAD v3: 15-87419490-T-C
gnomAD v4: 15-87419490-T-C
MyVariant Identifiers: chr15:g.87962721T>C (hg19) chr15:g.87419490T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419490T>C , CM000677.2:g.87419490T>C GRCh38
NC_000015.9:g.87962721T>C , CM000677.1:g.87962721T>C GRCh37
NC_000015.8:g.85763725T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-219A>G
XR_932585.1:n.340-219A>G
XR_001751647.1:n.617-219A>G
XR_932585.2:n.627-219A>G
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