Canonical Allele Identifier: CA1439212772
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578140A= , CM000666.2:g.12578140A= GRCh38
NC_000004.11:g.12579764A= , CM000666.1:g.12579764A= GRCh37
NC_000004.10:g.12188862A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31202T=
XR_001741374.1:n.254+44515T=
XR_925406.3:n.140+31202T=