Canonical Allele Identifier: CA1591798711
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354552C= , CM000667.2:g.152354552C= GRCh38
NC_000005.9:g.151734113C= , CM000667.1:g.151734113C= GRCh37
NC_000005.8:g.151714306C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16689C=
XR_944433.2:n.197+16689C=