Canonical Allele Identifier: CA1580179065
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002812C= , CM000667.2:g.126002812C= GRCh38
NC_000005.9:g.125338505C= , CM000667.1:g.125338505C= GRCh37
NC_000005.8:g.125366404C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3528G=
XR_948738.1:n.497+5728G=