Canonical Allele Identifier: CA2386425922
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890319T= , CM000683.2:g.32890319T= GRCh38
NC_000021.8:g.34262627T= , CM000683.1:g.34262627T= GRCh37
NC_000021.7:g.33184497T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937669.1:n.460-3259T=
XR_937669.2:n.1038-3259T=