Canonical Allele Identifier: CA11726849
Gene: CXCL9 HGNC NCBI
SDAD1-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.76001835A>G
GRCh37 chr4:g.76922988A>G
gnomAD v2:
4:76922988 A / G
gnomAD v3:
4:76001835 A / G
gnomAD v4:
chr4-76001835-A-G
Joint Max Group AF 0.91445533 (EAS)
Genomes Max Group AF 0.91728663 (EAS)
Exomes Max Group AF 0.84529165 (EAS)
dbSNP:
10336
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76001835A>G , CM000666.2:g.76001835A>G GRCh38
NC_000004.11:g.76922988A>G , CM000666.1:g.76922988A>G GRCh37
NC_000004.10:g.77142012A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264888.6:c.*1763T>C (CXCL9) MANE Select ENSP00000354901.4:n.*1763T>C
ENST00000264888.5:c.*1763T>C (CXCL9) ENSP00000354901.4:n.*1763T>C
NM_002416.2:c.*1763T>C (CXCL9) NP_002407.1:n.*1763T>C
NR_125906.1:n.816-3238A>G (SDAD1-AS1)
NM_002416.3:c.*1763T>C (CXCL9) MANE Select NP_002407.1:n.*1763T>C
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