Canonical Allele Identifier: CA619736704
Gene:

Linked Data

dbSNP Id: rs1004586465
gnomAD v2: 15-87962693-C-T
gnomAD v3: 15-87419462-C-T
gnomAD v4: 15-87419462-C-T
MyVariant Identifiers: chr15:g.87962693C>T (hg19) chr15:g.87419462C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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