Canonical Allele Identifier: CA1475277594
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597799T= , CM000666.2:g.89597799T= GRCh38
NC_000004.11:g.90518950T= , CM000666.1:g.90518950T= GRCh37
NC_000004.10:g.90737973T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9859T=
XR_938987.1:n.433-354T=
XR_938988.1:n.299-354T=
XR_938990.1:n.298+9859T=
XR_938991.1:n.298+9859T=
XR_938992.1:n.298+9859T=
XR_938994.1:n.643+9859T=
XR_938995.1:n.477+9859T=
XR_938996.1:n.298+9859T=
XR_938997.1:n.298+9859T=
XR_938986.2:n.323+9859T=
XR_938987.2:n.493-354T=