Canonical Allele Identifier: CA1563552069
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222760C= , CM000667.2:g.92222760C= GRCh38
NC_000005.9:g.91518577C= , CM000667.1:g.91518577C= GRCh37
NC_000005.8:g.91554333C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18076C=