Canonical Allele Identifier: CA1818149522
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999545G= , CM000670.2:g.126999545G= GRCh38
NC_000008.10:g.128011790G= , CM000670.1:g.128011790G= GRCh37
NC_000008.9:g.128080972G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7010G=