Canonical Allele Identifier: CA1369169859
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428097T= , CM000665.2:g.61428097T= GRCh38
NC_000003.11:g.61413771T= , CM000665.1:g.61413771T= GRCh37
NC_000003.10:g.61388811T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.165-411A=
XR_940893.1:n.164+417A=
XR_001740725.1:n.202+417A=
XR_940892.2:n.203-411A=