Canonical Allele Identifier: CA1282456465
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079702C= , CM000664.2:g.118079702C= GRCh38
NC_000002.11:g.118837278C= , CM000664.1:g.118837278C= GRCh37
NC_000002.10:g.118553748C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512305.1:c.697-2170G= XP_011510607.1:n.697-2170G=
XR_001739662.2:n.138+8549G=