Canonical Allele Identifier: CA1475277754
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89598130A= , CM000666.2:g.89598130A= GRCh38
NC_000004.11:g.90519281A= , CM000666.1:g.90519281A= GRCh37
NC_000004.10:g.90738304A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+10190A=
XR_938987.1:n.433-23A=
XR_938988.1:n.299-23A=
XR_938990.1:n.298+10190A=
XR_938991.1:n.298+10190A=
XR_938992.1:n.298+10190A=
XR_938994.1:n.643+10190A=
XR_938995.1:n.477+10190A=
XR_938996.1:n.298+10190A=
XR_938997.1:n.298+10190A=
XR_938986.2:n.323+10190A=
XR_938987.2:n.493-23A=