Canonical Allele Identifier: CA1439212494
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12577867T= , CM000666.2:g.12577867T= GRCh38
NC_000004.11:g.12579491T= , CM000666.1:g.12579491T= GRCh37
NC_000004.10:g.12188589T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31475A=
XR_001741374.1:n.254+44788A=
XR_925406.3:n.140+31475A=