Canonical Allele Identifier: CA304901017
Gene:

Linked Data

ClinVar Variation Id: 5408
ClinVar RCV Id: RCV000005739 RCV000005740 RCV000005741
dbSNP Id: rs4804803
gnomAD v2: 19-7812733-A-G
gnomAD v3: 19-7747847-A-G
gnomAD v4: 19-7747847-A-G
MyVariant Identifiers: chr19:g.7812733A>G (hg19) chr19:g.7747847A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7747847A>G , CM000681.2:g.7747847A>G GRCh38
NC_000019.9:g.7812733A>G , CM000681.1:g.7812733A>G GRCh37
NC_000019.8:g.7718733A>G NCBI36
NG_012167.1:g.4732T>C
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