Canonical Allele Identifier: CA2224227952
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56610665T= , CM000678.2:g.56610665T= GRCh38
NC_000016.9:g.56644577T= , CM000678.1:g.56644577T= GRCh37
NC_000016.8:g.55202078T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933616.1:n.605+651A=