Canonical Allele Identifier: CA13698471
Gene: SBNO1 HGNC NCBI

Linked Data

dbSNP Id: rs4759375
gnomAD v2: 12-123796238-C-T
gnomAD v3: 12-123311691-C-T
gnomAD v4: 12-123311691-C-T
MyVariant Identifiers: chr12:g.123796238C>T (hg19) chr12:g.123311691C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.123311691C>T , CM000674.2:g.123311691C>T GRCh38
NC_000012.11:g.123796238C>T , CM000674.1:g.123796238C>T GRCh37
NC_000012.10:g.122362191C>T NCBI36
NG_052874.1:g.58519G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000602398.3:c.3221-562G>A MANE Select ENSP00000473665.1:n.3221-562G>A
ENST00000267176.8:c.3218-562G>A ENSP00000267176.4:n.3218-562G>A
ENST00000420886.6:c.3221-562G>A ENSP00000387361.2:n.3221-562G>A
ENST00000602398.2:c.3221-562G>A ENSP00000473665.1:n.3221-562G>A
NM_001167856.1:c.3221-562G>A NP_001161328.1:n.3221-562G>A
NM_018183.3:c.3218-562G>A NP_060653.3:n.3218-562G>A
XM_005253572.2:c.3221-562G>A XP_005253629.1:n.3221-562G>A
XM_005253573.3:c.3221-562G>A XP_005253630.1:n.3221-562G>A
XM_005253575.2:c.3218-562G>A XP_005253632.1:n.3218-562G>A
XM_005253576.2:c.3218-562G>A XP_005253633.1:n.3218-562G>A
XM_006719473.2:c.3221-562G>A XP_006719536.1:n.3221-562G>A
XM_006719474.2:c.3221-562G>A XP_006719537.1:n.3221-562G>A
XM_011538533.1:c.3218-562G>A XP_011536835.1:n.3218-562G>A
XM_011538534.1:c.3116-562G>A XP_011536836.1:n.3116-562G>A
XM_011538535.1:c.3113-562G>A XP_011536837.1:n.3113-562G>A
NM_001167856.2:c.3221-562G>A NP_001161328.1:n.3221-562G>A
NM_018183.4:c.3218-562G>A NP_060653.3:n.3218-562G>A
NM_001167856.3:c.3221-562G>A MANE Select NP_001161328.1:n.3221-562G>A
NM_018183.5:c.3218-562G>A NP_060653.3:n.3218-562G>A
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