Canonical Allele Identifier: CA780108872
Gene:

Linked Data

dbSNP Id: rs1166515207
gnomAD v3: 18-49645742-A-G
gnomAD v4: 18-49645742-A-G
MyVariant Identifiers: chr18:g.47172112A>G (hg19) chr18:g.49645742A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645742A>G , CM000680.2:g.49645742A>G GRCh38
NC_000018.9:g.47172112A>G , CM000680.1:g.47172112A>G GRCh37
NC_000018.8:g.45426110A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935461.1:n.162-16292A>G
XR_001753446.1:n.898-16292A>G
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