Canonical Allele Identifier: CA14232780
Gene:

Linked Data

dbSNP Id: rs11644034
gnomAD v2: 16-85972612-G-A
gnomAD v3: 16-85939006-G-A
gnomAD v4: 16-85939006-G-A
MyVariant Identifiers: chr16:g.85972612G>A (hg19) chr16:g.85939006G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.85939006G>A , CM000678.2:g.85939006G>A GRCh38
NC_000016.9:g.85972612G>A , CM000678.1:g.85972612G>A GRCh37
NC_000016.8:g.84530113G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933852.1:n.466-6410G>A
XR_933853.1:n.466-6410G>A
Search 100 bp 5'
Search 100 bp 3'