gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.76021147A>T , CM000666.2:g.76021147A>T | GRCh38 |
| NC_000004.11:g.76942300A>T , CM000666.1:g.76942300A>T | GRCh37 |
| NC_000004.10:g.77161324A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000306602.3:c.*783T>A (CXCL10) MANE Select | ENSP00000305651.1:n.*783T>A | |
| ENST00000306602.2:c.*783T>A (CXCL10) | ENSP00000305651.1:n.*783T>A | |
| ENST00000341029.9:c.-10+9827A>T (ART3) | ENSP00000343843.5:n.-10+9827A>T | |
| ENST00000504914.5:c.-10+8904A>T (ART3) | ENSP00000421431.1:n.-10+8904A>T | |
| ENST00000510669.5:n.121+9827A>T (ART3) | ||
| ENST00000513122.5:c.-125+9827A>T (ART3) | ENSP00000422287.1:n.-125+9827A>T | |
| ENST00000513353.5:c.-44+9827A>T (ART3) | ENSP00000421345.1:n.-44+9827A>T | |
| NM_001130017.2:c.-10+9827A>T (ART3) | NP_001123489.1:n.-10+9827A>T | |
| NM_001565.3:c.*783T>A (CXCL10) | NP_001556.2:n.*783T>A | |
| XM_017008206.2:c.-44+9827A>T (ART3) | XP_016863695.1:n.-44+9827A>T | |
| XM_024454051.1:c.-10+9827A>T (ART3) | XP_024309819.1:n.-10+9827A>T | |
| XM_024454052.1:c.-125+9827A>T (ART3) | XP_024309820.1:n.-125+9827A>T | |
| XM_024454053.1:c.-136+9827A>T (ART3) | XP_024309821.1:n.-136+9827A>T | |
| XM_024454063.1:c.-10+9827A>T (ART3) | XP_024309831.1:n.-10+9827A>T | |
| NM_001565.4:c.*783T>A (CXCL10) MANE Select | NP_001556.2:n.*783T>A | |
| NM_001130017.3:c.-10+9827A>T (ART3) | NP_001123489.1:n.-10+9827A>T | |
| NM_001377177.1:c.-10+9827A>T (ART3) | NP_001364106.1:n.-10+9827A>T | |
| NM_001377181.1:c.-10+9827A>T (ART3) | NP_001364110.1:n.-10+9827A>T | |
| NM_001377183.1:c.-10+9827A>T (ART3) | NP_001364112.1:n.-10+9827A>T | |
| NR_168520.1:n.1019T>A (CXCL10) |