Canonical Allele Identifier: CA1769514605
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735058A= , CM000670.2:g.20735058A= GRCh38
NC_000008.10:g.20592569A= , CM000670.1:g.20592569A= GRCh37
NC_000008.9:g.20636849A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55388A=