Canonical Allele Identifier: CA1282459308
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118086902C= , CM000664.2:g.118086902C= GRCh38
NC_000002.11:g.118844478C= , CM000664.1:g.118844478C= GRCh37
NC_000002.10:g.118560948C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.696+1158G= XP_011510607.1:n.696+1158G=
XR_001739662.2:n.138+1349G=