Canonical Allele Identifier: CA2065107417
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398733T= , CM000674.2:g.115398733T= GRCh38
NC_000012.11:g.115836538T= , CM000674.1:g.115836538T= GRCh37
NC_000012.10:g.114320921T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8362A=
XR_945389.2:n.701+8362A=