Canonical Allele Identifier: CA2607842099
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs2108850624
gnomAD v4: 3-143785581-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143785581A>G , CM000665.2:g.143785581A>G GRCh38
NC_000003.11:g.143504423A>G , CM000665.1:g.143504423A>G GRCh37
NC_000003.10:g.144987113A>G NCBI36
NG_017077.1:g.67951T>C
NG_017077.2:g.67951T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.533+9420T>C MANE Select ENSP00000320246.6:n.533+9420T>C
ENST00000316549.10:c.533+9420T>C ENSP00000320246.6:n.533+9420T>C
ENST00000474727.2:c.*144+9420T>C ENSP00000419090.2:n.*144+9420T>C
NM_173653.3:c.533+9420T>C NP_775924.1:n.533+9420T>C
XM_011512704.1:c.533+9420T>C XP_011511006.1:n.533+9420T>C
XM_011512704.3:c.533+9420T>C XP_011511006.1:n.533+9420T>C
XM_017006202.2:c.533+9420T>C XP_016861691.1:n.533+9420T>C
XM_017006203.1:c.182+9420T>C XP_016861692.1:n.182+9420T>C
NM_173653.4:c.533+9420T>C MANE Select NP_775924.1:n.533+9420T>C
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