Canonical Allele Identifier: CA1369169797
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61427969A= , CM000665.2:g.61427969A= GRCh38
NC_000003.11:g.61413643A= , CM000665.1:g.61413643A= GRCh37
NC_000003.10:g.61388683A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.165-283T=
XR_940893.1:n.164+545T=
XR_001740725.1:n.202+545T=
XR_940892.2:n.203-283T=