Canonical Allele Identifier: CA1223909920
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068624G= , CM000663.2:g.224068624G= GRCh38
NC_000001.10:g.224256326G= , CM000663.1:g.224256326G= GRCh37
NC_000001.9:g.222322949G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+970G=
XR_001737824.1:n.242+970G=