Canonical Allele Identifier: CA10602355
Gene:

Linked Data

ClinVar Variation Id: 12323
ClinVar RCV Id: RCV000013116
dbSNP Id: rs886037621
gnomAD v2: 8-11422122-G-T
gnomAD v3: 8-11564613-G-T
gnomAD v4: 8-11564613-G-T
MyVariant Identifiers: chr8:g.11422122G>T (hg19) chr8:g.11564613G>T (hg38)
PubMed: PMID:19667185
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564613G>T , CM000670.2:g.11564613G>T GRCh38
NC_000008.10:g.11422122G>T , CM000670.1:g.11422122G>T GRCh37
NC_000008.9:g.11459531G>T NCBI36
NG_023543.1:g.75602G>T
NG_023543.2:g.75602G>T
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