Canonical Allele Identifier: CA13647861
Gene: SUOX HGNC NCBI

Linked Data

dbSNP Id: rs7297662
gnomAD v2: 12-56395378-G-A
gnomAD v3: 12-56001594-G-A
gnomAD v4: 12-56001594-G-A
MyVariant Identifiers: chr12:g.56395378G>A (hg19) chr12:g.56001594G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56001594G>A , CM000674.2:g.56001594G>A GRCh38
NC_000012.11:g.56395378G>A , CM000674.1:g.56395378G>A GRCh37
NC_000012.10:g.54681645G>A NCBI36
NG_008136.1:g.9336G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000266971.8:c.-10-618G>A MANE Select ENSP00000266971.3:n.-10-618G>A
ENST00000266971.7:c.-10-618G>A ENSP00000266971.3:n.-10-618G>A
ENST00000356124.8:c.-10-618G>A ENSP00000348440.4:n.-10-618G>A
ENST00000394109.7:c.-628G>A ENSP00000377668.3:n.-628G>A
ENST00000394115.6:c.-10-618G>A ENSP00000377674.2:n.-10-618G>A
ENST00000546833.5:c.-73-292G>A ENSP00000449872.1:n.-73-292G>A
ENST00000547586.5:c.-10-618G>A ENSP00000448637.1:n.-10-618G>A
ENST00000548274.5:c.-11+122G>A ENSP00000450245.1:n.-11+122G>A
ENST00000550121.5:n.449-213G>A
ENST00000550340.5:n.54-618G>A
ENST00000550478.5:n.131-618G>A
ENST00000551698.5:n.191-618G>A
ENST00000551841.6:c.-10-618G>A ENSP00000449443.1:n.-10-618G>A
ENST00000552258.5:c.-10-618G>A ENSP00000450049.1:n.-10-618G>A
ENST00000552363.5:n.82-2024G>A
ENST00000552813.5:n.132-618G>A
NM_000456.2:c.-10-618G>A NP_000447.2:n.-10-618G>A
NM_001032386.1:c.-10-618G>A NP_001027558.1:n.-10-618G>A
NM_001032387.1:c.-10-618G>A NP_001027559.1:n.-10-618G>A
XM_005269112.1:c.-52-292G>A XP_005269169.1:n.-52-292G>A
XM_017019905.2:c.-52-292G>A XP_016875394.1:n.-52-292G>A
XM_017019906.1:c.-52-292G>A XP_016875395.1:n.-52-292G>A
XM_017019907.2:c.-10-618G>A XP_016875396.1:n.-10-618G>A
XM_017019908.1:c.-10-618G>A XP_016875397.1:n.-10-618G>A
XM_024449167.1:c.-52-292G>A XP_024304935.1:n.-52-292G>A
NM_001032386.2:c.-10-618G>A MANE Select NP_001027558.1:n.-10-618G>A
NM_000456.3:c.-10-618G>A NP_000447.2:n.-10-618G>A
NM_001032387.2:c.-10-618G>A NP_001027559.1:n.-10-618G>A
Search 100 bp 5'
Search 100 bp 3'