Canonical Allele Identifier: CA2762575088
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597904T>A , CM000666.2:g.89597904T>A GRCh38
NC_000004.11:g.90519055T>A , CM000666.1:g.90519055T>A GRCh37
NC_000004.10:g.90738078T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9964T>A
XR_938987.1:n.433-249T>A
XR_938988.1:n.299-249T>A
XR_938990.1:n.298+9964T>A
XR_938991.1:n.298+9964T>A
XR_938992.1:n.298+9964T>A
XR_938994.1:n.643+9964T>A
XR_938995.1:n.477+9964T>A
XR_938996.1:n.298+9964T>A
XR_938997.1:n.298+9964T>A
XR_938986.2:n.323+9964T>A
XR_938987.2:n.493-249T>A
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