Canonical Allele Identifier: CA1496041092
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134616564T>G , CM000666.2:g.134616564T>G GRCh38
NC_000004.11:g.135537719T>G , CM000666.1:g.135537719T>G GRCh37
NC_000004.10:g.135757169T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.411-23016T>G
XR_939214.1:n.393-23016T>G
XR_939214.2:n.393-23016T>G