Canonical Allele Identifier: CA2002576381
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442788A= , CM000673.2:g.116442788A= GRCh38
NC_000011.9:g.116313505A= , CM000673.1:g.116313505A= GRCh37
NC_000011.8:g.115818715A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748403.1:n.349+31089T=