Canonical Allele Identifier: CA2008080768
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128455537A= , CM000673.2:g.128455537A= GRCh38
NC_000011.9:g.128325432A= , CM000673.1:g.128325432A= GRCh37
NC_000011.8:g.127830642A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948164.1:n.4257A=
XR_948165.1:n.3467+790A=