Canonical Allele Identifier: CA1468603658
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74304335T= , CM000666.2:g.74304335T= GRCh38
NC_000004.11:g.75170052T= , CM000666.1:g.75170052T= GRCh37
NC_000004.10:g.75388916T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938877.1:n.120-25557A=
XR_938877.2:n.126-25557A=