Canonical Allele Identifier: CA14081494
Gene:

Linked Data

ClinVar Variation Id: 1168574
ClinVar RCV Id: RCV001518931
dbSNP Id: rs12899331
gnomAD v2: 15-55801094-A-G
gnomAD v3: 15-55508896-A-G
gnomAD v4: 15-55508896-A-G
MyVariant Identifiers: chr15:g.55801094A>G (hg19) chr15:g.55508896A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.55508896A>G , CM000677.2:g.55508896A>G GRCh38
NC_000015.9:g.55801094A>G , CM000677.1:g.55801094A>G GRCh37
NC_000015.8:g.53588386A>G NCBI36
NG_021213.1:g.4339T>C
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