Canonical Allele Identifier: CA1620168900
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33794465G= , CM000668.2:g.33794465G= GRCh38
NC_000006.11:g.33762242G= , CM000668.1:g.33762242G= GRCh37
NC_000006.10:g.33870220G= NCBI36
NG_053042.1:g.4810C=

Transcript Alleles

HGVS Amino-acid Change
XR_001744088.1:n.81+1310G=
XR_926707.1:n.1443+1310G=
XR_926707.2:n.81+1310G=
XR_926708.1:n.227+1310G=
XR_926709.1:n.1443+1310G=