Canonical Allele Identifier: CA2255112038
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237346G= , CM000679.2:g.30237346G= GRCh38
NC_000017.10:g.28564364G= , CM000679.1:g.28564364G= GRCh37
NC_000017.9:g.25588490G= NCBI36
NG_011747.2:g.3591C=

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+276G=
XR_001752824.1:n.280+276G=