Canonical Allele Identifier: CA14173831
Gene:

Linked Data

dbSNP Id: rs11636768
gnomAD v2: 15-87695511-G-A
gnomAD v3: 15-87152280-G-A
gnomAD v4: 15-87152280-G-A
MyVariant Identifiers: chr15:g.87695511G>A (hg19) chr15:g.87152280G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152280G>A , CM000677.2:g.87152280G>A GRCh38
NC_000015.9:g.87695511G>A , CM000677.1:g.87695511G>A GRCh37
NC_000015.8:g.85496515G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932582.1:n.167-25947G>A
XR_932582.2:n.167-25947G>A
Search 100 bp 5'
Search 100 bp 3'