Canonical Allele Identifier: CA1439212787
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578147T= , CM000666.2:g.12578147T= GRCh38
NC_000004.11:g.12579771T= , CM000666.1:g.12579771T= GRCh37
NC_000004.10:g.12188869T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31195A=
XR_001741374.1:n.254+44508A=
XR_925406.3:n.140+31195A=