Canonical Allele Identifier: CA1439212801
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578172A= , CM000666.2:g.12578172A= GRCh38
NC_000004.11:g.12579796A= , CM000666.1:g.12579796A= GRCh37
NC_000004.10:g.12188894A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31170T=
XR_001741374.1:n.254+44483T=
XR_925406.3:n.140+31170T=