Canonical Allele Identifier: CA1282456411
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079586A= , CM000664.2:g.118079586A= GRCh38
NC_000002.11:g.118837162A= , CM000664.1:g.118837162A= GRCh37
NC_000002.10:g.118553632A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2054T= XP_011510607.1:n.697-2054T=
XR_001739662.2:n.138+8665T=