Canonical Allele Identifier: CA220638178
Gene:

Linked Data

dbSNP Id: rs112133182
MyVariant Identifiers: chr11:g.34781058T>A (hg19) chr11:g.34759511T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759511T>A , CM000673.2:g.34759511T>A GRCh38
NC_000011.9:g.34781058T>A , CM000673.1:g.34781058T>A GRCh37
NC_000011.8:g.34737634T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4904T>A
XR_931188.1:n.693+4904T>A
XR_931189.1:n.854+4904T>A
XR_931190.1:n.639+4904T>A
XR_931191.1:n.689+4904T>A
XR_001748174.1:n.855+4904T>A
XR_001748176.1:n.1016+4904T>A
XR_002957246.1:n.639+4904T>A
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