Canonical Allele Identifier: CA1320446142
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033166G= , CM000664.2:g.200033166G= GRCh38
NC_000002.11:g.200897889G= , CM000664.1:g.200897889G= GRCh37
NC_000002.10:g.200606134G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22270C=