Canonical Allele Identifier: CA13060692

Gene: QSOX2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136220024G>T , CM000671.2:g.136220024G>T	GRCh38
NC_000009.11:g.139111870G>T , CM000671.1:g.139111870G>T	GRCh37
NC_000009.10:g.138251691G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358701.10:c.822-860C>A MANE Select	ENSP00000351536.5:n.822-860C>A
ENST00000358701.9:c.822-860C>A	ENSP00000351536.5:n.822-860C>A
ENST00000455222.1:c.124-860C>A
ENST00000616829.4:c.822-860C>A	ENSP00000483961.1:n.822-860C>A
NM_181701.3:c.822-860C>A	NP_859052.3:n.822-860C>A
NM_181701.4:c.822-860C>A MANE Select	NP_859052.3:n.822-860C>A