Canonical Allele Identifier: CA2793754339
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442707A>T , CM000673.2:g.116442707A>T GRCh38
NC_000011.9:g.116313424A>T , CM000673.1:g.116313424A>T GRCh37
NC_000011.8:g.115818634A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748403.1:n.349+31170T>A