Canonical Allele Identifier: CA1282456444
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079663T= , CM000664.2:g.118079663T= GRCh38
NC_000002.11:g.118837239T= , CM000664.1:g.118837239T= GRCh37
NC_000002.10:g.118553709T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2131A= XP_011510607.1:n.697-2131A=
XR_001739662.2:n.138+8588A=