Canonical Allele Identifier: CA201562599
Gene: QSOX2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136229894A>T , CM000671.2:g.136229894A>T GRCh38
NC_000009.11:g.139121740A>T , CM000671.1:g.139121740A>T GRCh37
NC_000009.10:g.138261561A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358701.10:c.329-3020T>A MANE Select ENSP00000351536.5:n.329-3020T>A
ENST00000358701.9:c.329-3020T>A ENSP00000351536.5:n.329-3020T>A
ENST00000616829.4:c.329-3020T>A ENSP00000483961.1:n.329-3020T>A
NM_181701.3:c.329-3020T>A NP_859052.3:n.329-3020T>A
NM_181701.4:c.329-3020T>A MANE Select NP_859052.3:n.329-3020T>A