Canonical Allele Identifier: CA1320446165
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033213G= , CM000664.2:g.200033213G= GRCh38
NC_000002.11:g.200897936G= , CM000664.1:g.200897936G= GRCh37
NC_000002.10:g.200606181G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22317C=