Canonical Allele Identifier: CA1282456416
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079600T= , CM000664.2:g.118079600T= GRCh38
NC_000002.11:g.118837176T= , CM000664.1:g.118837176T= GRCh37
NC_000002.10:g.118553646T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2068A= XP_011510607.1:n.697-2068A=
XR_001739662.2:n.138+8651A=