Canonical Allele Identifier: CA1282456420
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079605G= , CM000664.2:g.118079605G= GRCh38
NC_000002.11:g.118837181G= , CM000664.1:g.118837181G= GRCh37
NC_000002.10:g.118553651G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2073C= XP_011510607.1:n.697-2073C=
XR_001739662.2:n.138+8646C=