Canonical Allele Identifier: CA1818149990
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999823G= , CM000670.2:g.126999823G= GRCh38
NC_000008.10:g.128012068G= , CM000670.1:g.128012068G= GRCh37
NC_000008.9:g.128081250G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6732G=