Canonical Allele Identifier: CA1054416034
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs2031970151
gnomAD v3: 3-143337622-A-T
gnomAD v4: 3-143337622-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143337622A>T , CM000665.2:g.143337622A>T GRCh38
NC_000003.11:g.143056464A>T , CM000665.1:g.143056464A>T GRCh37
NC_000003.10:g.144539154A>T NCBI36
NG_017077.1:g.515910T>A
NG_017077.2:g.515910T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1604+25862T>A MANE Select ENSP00000320246.6:n.1604+25862T>A
ENST00000316549.10:c.1604+25862T>A ENSP00000320246.6:n.1604+25862T>A
NM_173653.3:c.1604+25862T>A NP_775924.1:n.1604+25862T>A
XM_011512703.1:c.956+25862T>A XP_011511005.1:n.956+25862T>A
XM_011512703.3:c.956+25862T>A XP_011511005.1:n.956+25862T>A
XM_017006202.2:c.1711+25755T>A XP_016861691.1:n.1711+25755T>A
XM_017006203.1:c.1253+25862T>A XP_016861692.1:n.1253+25862T>A
NM_173653.4:c.1604+25862T>A MANE Select NP_775924.1:n.1604+25862T>A
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