Canonical Allele Identifier: CA303945600
Gene:

Linked Data

ClinVar Variation Id: 1209350
ClinVar RCV Id: RCV001577984
dbSNP Id: rs17216677
gnomAD v2: 19-856301-G-A
gnomAD v3: 19-856301-G-A
gnomAD v4: 19-856301-G-A
MyVariant Identifiers: chr19:g.856301G>A (hg19) chr19:g.856301G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.856301G>A , CM000681.2:g.856301G>A GRCh38
NC_000019.9:g.856301G>A , CM000681.1:g.856301G>A GRCh37
NC_000019.8:g.807301G>A NCBI36
NG_007274.1:g.1637G>A , LRG_46:g.1637G>A
NG_009627.1:g.9011G>A , LRG_57:g.9011G>A
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