Canonical Allele Identifier: CA15313106

Gene: CXCL10 ART3

Linked Data

• dbSNP Id: rs3921
• gnomAD v2: 4-76942943-C-G
• gnomAD v3: 4-76021790-C-G
• gnomAD v4: 4-76021790-C-G
• MyVariant Identifiers: chr4:g.76942943C>G (hg19) ; chr4:g.76021790C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76021790C>G , CM000666.2:g.76021790C>G	GRCh38
NC_000004.11:g.76942943C>G , CM000666.1:g.76942943C>G	GRCh37
NC_000004.10:g.77161967C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306602.3:c.*140G>C (CXCL10) MANE Select	ENSP00000305651.1:n.*140G>C
ENST00000306602.2:c.*140G>C (CXCL10)	ENSP00000305651.1:n.*140G>C
ENST00000341029.9:c.-10+10470C>G (ART3)	ENSP00000343843.5:n.-10+10470C>G
ENST00000504914.5:c.-10+9547C>G (ART3)	ENSP00000421431.1:n.-10+9547C>G
ENST00000510669.5:n.121+10470C>G (ART3)
ENST00000513122.5:c.-125+10470C>G (ART3)	ENSP00000422287.1:n.-125+10470C>G
ENST00000513353.5:c.-44+10470C>G (ART3)	ENSP00000421345.1:n.-44+10470C>G
NM_001130017.2:c.-10+10470C>G (ART3)	NP_001123489.1:n.-10+10470C>G
NM_001565.3:c.*140G>C (CXCL10)	NP_001556.2:n.*140G>C
XM_017008206.2:c.-44+10470C>G (ART3)	XP_016863695.1:n.-44+10470C>G
XM_024454051.1:c.-10+10470C>G (ART3)	XP_024309819.1:n.-10+10470C>G
XM_024454052.1:c.-125+10470C>G (ART3)	XP_024309820.1:n.-125+10470C>G
XM_024454053.1:c.-136+10470C>G (ART3)	XP_024309821.1:n.-136+10470C>G
XM_024454063.1:c.-10+10470C>G (ART3)	XP_024309831.1:n.-10+10470C>G
NM_001565.4:c.*140G>C (CXCL10) MANE Select	NP_001556.2:n.*140G>C
NM_001130017.3:c.-10+10470C>G (ART3)	NP_001123489.1:n.-10+10470C>G
NM_001377177.1:c.-10+10470C>G (ART3)	NP_001364106.1:n.-10+10470C>G
NM_001377181.1:c.-10+10470C>G (ART3)	NP_001364110.1:n.-10+10470C>G
NM_001377183.1:c.-10+10470C>G (ART3)	NP_001364112.1:n.-10+10470C>G
NR_168520.1:n.376G>C (CXCL10)