Canonical Allele Identifier: CA1475277610
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597842C= , CM000666.2:g.89597842C= GRCh38
NC_000004.11:g.90518993C= , CM000666.1:g.90518993C= GRCh37
NC_000004.10:g.90738016C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9902C=
XR_938987.1:n.433-311C=
XR_938988.1:n.299-311C=
XR_938990.1:n.298+9902C=
XR_938991.1:n.298+9902C=
XR_938992.1:n.298+9902C=
XR_938994.1:n.643+9902C=
XR_938995.1:n.477+9902C=
XR_938996.1:n.298+9902C=
XR_938997.1:n.298+9902C=
XR_938986.2:n.323+9902C=
XR_938987.2:n.493-311C=