Canonical Allele Identifier: CA1305906790
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260553A= , CM000664.2:g.168260553A= GRCh38
NC_000002.11:g.169117063A= , CM000664.1:g.169117063A= GRCh37
NC_000002.10:g.168825309A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4543A=
XR_001739764.1:n.318-4543A=
XR_001739765.1:n.436-4543A=