Canonical Allele Identifier: CA1784292597
Community Standard Title: NC_000008.11:g.52772301T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.52772301T= , CM000670.2:g.52772301T= GRCh38
NC_000008.10:g.53684861T= , CM000670.1:g.53684861T= GRCh37
NC_000008.9:g.53847414T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745898.1:n.685+2206T=
XR_928875.1:n.687+2206T=
XR_928876.1:n.1042+2206T=