Canonical Allele Identifier: CA13060692
Gene: QSOX2 HGNC NCBI

Linked Data

dbSNP Id: rs7849585

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