Canonical Allele Identifier: CA1905920024
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318673G= , CM000672.2:g.43318673G= GRCh38
NC_000010.10:g.43814121G= , CM000672.1:g.43814121G= GRCh37
NC_000010.9:g.43134127G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945902.1:n.108+78G=
XR_945902.2:n.198+78G=