Canonical Allele Identifier: CA1948159656
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444569T= , CM000673.2:g.2444569T= GRCh38
NC_000011.9:g.2465799T= , CM000673.1:g.2465799T= GRCh37
NC_000011.8:g.2422375T= NCBI36
NG_008935.1:g.4579T= , LRG_287:g.4579T=

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.2A=