Canonical Allele Identifier: CA1439212662
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578044A= , CM000666.2:g.12578044A= GRCh38
NC_000004.11:g.12579668A= , CM000666.1:g.12579668A= GRCh37
NC_000004.10:g.12188766A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31298T=
XR_001741374.1:n.254+44611T=
XR_925406.3:n.140+31298T=