Canonical Allele Identifier: CA2065107326
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398652G= , CM000674.2:g.115398652G= GRCh38
NC_000012.11:g.115836457G= , CM000674.1:g.115836457G= GRCh37
NC_000012.10:g.114320840G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945389.1:n.697+8443C=
XR_945389.2:n.701+8443C=