Canonical Allele Identifier: CA220643982
Gene:

Linked Data

dbSNP Id: rs933271131
MyVariant Identifiers: chr11:g.34834013C>G (hg19) chr11:g.34812466C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812466C>G , CM000673.2:g.34812466C>G GRCh38
NC_000011.9:g.34834013C>G , CM000673.1:g.34834013C>G GRCh37
NC_000011.8:g.34790589C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57859C>G
XR_931188.1:n.693+57859C>G
XR_931189.1:n.854+57859C>G
XR_931190.1:n.639+57859C>G
XR_931191.1:n.689+57859C>G
XR_001748174.1:n.855+57859C>G
XR_001748176.1:n.1016+57859C>G
XR_002957246.1:n.639+57859C>G
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