Canonical Allele Identifier: CA592700155
Gene:

Linked Data

dbSNP Id: rs1179720590
gnomAD v2: 10-30490776-A-G
gnomAD v3: 10-30201847-A-G
gnomAD v4: 10-30201847-A-G
MyVariant Identifiers: chr10:g.30490776A>G (hg19) chr10:g.30201847A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201847A>G , CM000672.2:g.30201847A>G GRCh38
NC_000010.10:g.30490776A>G , CM000672.1:g.30490776A>G GRCh37
NC_000010.9:g.30530782A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1640A>G
XR_930791.2:n.1449-1640A>G
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