Canonical Allele Identifier: CA1591798742
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152354613T= , CM000667.2:g.152354613T= GRCh38
NC_000005.9:g.151734174T= , CM000667.1:g.151734174T= GRCh37
NC_000005.8:g.151714367T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944433.1:n.196+16750T=
XR_944433.2:n.197+16750T=