Canonical Allele Identifier: CA2065107311
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398638A= , CM000674.2:g.115398638A= GRCh38
NC_000012.11:g.115836443A= , CM000674.1:g.115836443A= GRCh37
NC_000012.10:g.114320826A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8457T=
XR_945389.2:n.701+8457T=