Canonical Allele Identifier: CA1369169813
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61427997G= , CM000665.2:g.61427997G= GRCh38
NC_000003.11:g.61413671G= , CM000665.1:g.61413671G= GRCh37
NC_000003.10:g.61388711G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.165-311C=
XR_940893.1:n.164+517C=
XR_001740725.1:n.202+517C=
XR_940892.2:n.203-311C=