Canonical Allele Identifier: CA2065107292
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398629A= , CM000674.2:g.115398629A= GRCh38
NC_000012.11:g.115836434A= , CM000674.1:g.115836434A= GRCh37
NC_000012.10:g.114320817A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8466T=
XR_945389.2:n.701+8466T=