Canonical Allele Identifier: CA2226008614
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.60428792A>T , CM000678.2:g.60428792A>T GRCh38
NC_000016.9:g.60462696A>T , CM000678.1:g.60462696A>T GRCh37
NC_000016.8:g.59020197A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_243457.2:n.376-43944A>T
XR_933651.1:n.539-43944A>T
XR_933652.1:n.602-43944A>T
XR_933653.1:n.313-43944A>T
XR_001752229.1:n.539-43944A>T
XR_001752230.1:n.516-43944A>T
XR_001752231.1:n.313-43944A>T
XR_002957906.1:n.804-43944A>T