Canonical Allele Identifier: CA675841057
Gene:

Linked Data

dbSNP Id: rs1363096054
gnomAD v3: 11-34812537-C-T
gnomAD v4: 11-34812537-C-T
MyVariant Identifiers: chr11:g.34834084C>T (hg19) chr11:g.34812537C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812537C>T , CM000673.2:g.34812537C>T GRCh38
NC_000011.9:g.34834084C>T , CM000673.1:g.34834084C>T GRCh37
NC_000011.8:g.34790660C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57930C>T
XR_931188.1:n.693+57930C>T
XR_931189.1:n.854+57930C>T
XR_931190.1:n.639+57930C>T
XR_931191.1:n.689+57930C>T
XR_001748174.1:n.855+57930C>T
XR_001748176.1:n.1016+57930C>T
XR_002957246.1:n.639+57930C>T
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