Canonical Allele Identifier: CA1369169843
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428064G= , CM000665.2:g.61428064G= GRCh38
NC_000003.11:g.61413738G= , CM000665.1:g.61413738G= GRCh37
NC_000003.10:g.61388778G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.165-378C=
XR_940893.1:n.164+450C=
XR_001740725.1:n.202+450C=
XR_940892.2:n.203-378C=