Canonical Allele Identifier: CA2791024200
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812381T>A , CM000673.2:g.34812381T>A GRCh38
NC_000011.9:g.34833928T>A , CM000673.1:g.34833928T>A GRCh37
NC_000011.8:g.34790504T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57774T>A
XR_931188.1:n.693+57774T>A
XR_931189.1:n.854+57774T>A
XR_931190.1:n.639+57774T>A
XR_931191.1:n.689+57774T>A
XR_001748174.1:n.855+57774T>A
XR_001748176.1:n.1016+57774T>A
XR_002957246.1:n.639+57774T>A
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