Canonical Allele Identifier: CA1595159328
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580895G= , CM000667.2:g.159580895G= GRCh38
NC_000005.9:g.159007903G= , CM000667.1:g.159007903G= GRCh37
NC_000005.8:g.158940481G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+460G=
XR_941140.1:n.2075+460G=
XR_941141.1:n.570+460G=
XR_941139.2:n.2229+460G=