Canonical Allele Identifier: CA1439212868
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578242T= , CM000666.2:g.12578242T= GRCh38
NC_000004.11:g.12579866T= , CM000666.1:g.12579866T= GRCh37
NC_000004.10:g.12188964T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31100A=
XR_001741374.1:n.254+44413A=
XR_925406.3:n.140+31100A=