Canonical Allele Identifier: CA1427629887
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931553T= , CM000665.2:g.187931553T= GRCh38
NC_000003.11:g.187649341T= , CM000665.1:g.187649341T= GRCh37
NC_000003.10:g.189132035T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1361A=