Canonical Allele Identifier: CA1580179029
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002724C= , CM000667.2:g.126002724C= GRCh38
NC_000005.9:g.125338417C= , CM000667.1:g.125338417C= GRCh37
NC_000005.8:g.125366316C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3616G=
XR_948738.1:n.497+5816G=