Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.76001835A>C , CM000666.2:g.76001835A>C | GRCh38 |
| NC_000004.11:g.76922988A>C , CM000666.1:g.76922988A>C | GRCh37 |
| NC_000004.10:g.77142012A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002416.3:c.*1763T>G (CXCL9) MANE Select | NP_002407.1:n.*1763T>G |
| ENST00000264888.6:c.*1763T>G (CXCL9) MANE Select | ENSP00000354901.4:n.*1763T>G |
| NM_002416.2:c.*1763T>G (CXCL9) | NP_002407.1:n.*1763T>G |
| NR_125906.1:n.816-3238A>C (SDAD1-AS1) | |
| ENST00000264888.5:c.*1763T>G (CXCL9) | ENSP00000354901.4:n.*1763T>G |