Canonical Allele Identifier: CA1369169773
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61427911C= , CM000665.2:g.61427911C= GRCh38
NC_000003.11:g.61413585C= , CM000665.1:g.61413585C= GRCh37
NC_000003.10:g.61388625C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940892.1:n.165-225G=
XR_940893.1:n.164+603G=
XR_001740725.1:n.202+603G=
XR_940892.2:n.203-225G=