Canonical Allele Identifier: CA14109708
Gene:

Linked Data

dbSNP Id: rs8024343
gnomAD v2: 15-87710066-A-T
gnomAD v3: 15-87166835-A-T
gnomAD v4: 15-87166835-A-T
MyVariant Identifiers: chr15:g.87710066A>T (hg19) chr15:g.87166835A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87166835A>T , CM000677.2:g.87166835A>T GRCh38
NC_000015.9:g.87710066A>T , CM000677.1:g.87710066A>T GRCh37
NC_000015.8:g.85511070A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932582.1:n.167-11392A>T
XR_932582.2:n.167-11392A>T
Search 100 bp 5'
Search 100 bp 3'