Canonical Allele Identifier: CA1369169892
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61428155G= , CM000665.2:g.61428155G= GRCh38
NC_000003.11:g.61413829G= , CM000665.1:g.61413829G= GRCh37
NC_000003.10:g.61388869G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.164+359C=
XR_940893.1:n.164+359C=
XR_001740725.1:n.202+359C=
XR_940892.2:n.202+359C=