Canonical Allele Identifier: CA2767457778
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222955C>A , CM000667.2:g.92222955C>A GRCh38
NC_000005.9:g.91518772C>A , CM000667.1:g.91518772C>A GRCh37
NC_000005.8:g.91554528C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948565.1:n.394+18271C>A