Canonical Allele Identifier: CA1320479877
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200130964C= , CM000664.2:g.200130964C= GRCh38
NC_000002.11:g.200995687C= , CM000664.1:g.200995687C= GRCh37
NC_000002.10:g.200703932C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.177+43606G=