Canonical Allele Identifier: CA2364010690
Community Standard Title: NC_000020.11:g.40640434T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.40640434T= , CM000682.2:g.40640434T= GRCh38
NC_000020.10:g.39269074T= , CM000682.1:g.39269074T= GRCh37
NC_000020.9:g.38702488T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754596.1:n.165+100A=
XR_001754597.1:n.180+3477A=