Canonical Allele Identifier: CA2767457777
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222942C>A , CM000667.2:g.92222942C>A GRCh38
NC_000005.9:g.91518759C>A , CM000667.1:g.91518759C>A GRCh37
NC_000005.8:g.91554515C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18258C>A