Canonical Allele Identifier: CA1818149788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999706G= , CM000670.2:g.126999706G= GRCh38
NC_000008.10:g.128011951G= , CM000670.1:g.128011951G= GRCh37
NC_000008.9:g.128081133G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6849G=