Canonical Allele Identifier: CA2762575092
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89598052A>T , CM000666.2:g.89598052A>T GRCh38
NC_000004.11:g.90519203A>T , CM000666.1:g.90519203A>T GRCh37
NC_000004.10:g.90738226A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+10112A>T
XR_938987.1:n.433-101A>T
XR_938988.1:n.299-101A>T
XR_938990.1:n.298+10112A>T
XR_938991.1:n.298+10112A>T
XR_938992.1:n.298+10112A>T
XR_938994.1:n.643+10112A>T
XR_938995.1:n.477+10112A>T
XR_938996.1:n.298+10112A>T
XR_938997.1:n.298+10112A>T
XR_938986.2:n.323+10112A>T
XR_938987.2:n.493-101A>T
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