Canonical Allele Identifier: CA1369169920
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428224C= , CM000665.2:g.61428224C= GRCh38
NC_000003.11:g.61413898C= , CM000665.1:g.61413898C= GRCh37
NC_000003.10:g.61388938C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.164+290G=
XR_940893.1:n.164+290G=
XR_001740725.1:n.202+290G=
XR_940892.2:n.202+290G=