Canonical Allele Identifier: CA1563552050
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222716T= , CM000667.2:g.92222716T= GRCh38
NC_000005.9:g.91518533T= , CM000667.1:g.91518533T= GRCh37
NC_000005.8:g.91554289T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18032T=