Canonical Allele Identifier: CA2065107405
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398724C= , CM000674.2:g.115398724C= GRCh38
NC_000012.11:g.115836529C= , CM000674.1:g.115836529C= GRCh37
NC_000012.10:g.114320912C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8371G=
XR_945389.2:n.701+8371G=