Canonical Allele Identifier: CA1580179064
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002808C= , CM000667.2:g.126002808C= GRCh38
NC_000005.9:g.125338501C= , CM000667.1:g.125338501C= GRCh37
NC_000005.8:g.125366400C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3532G=
XR_948738.1:n.497+5732G=