Canonical Allele Identifier: CA99820280

Gene: CXCL10 ART3

Linked Data

• dbSNP Id: rs35795399
• gnomAD v2: 4-76942677-T-C
• gnomAD v3: 4-76021524-T-C
• gnomAD v4: 4-76021524-T-C
• MyVariant Identifiers: chr4:g.76942677T>C (hg19) ; chr4:g.76021524T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76021524T>C , CM000666.2:g.76021524T>C	GRCh38
NC_000004.11:g.76942677T>C , CM000666.1:g.76942677T>C	GRCh37
NC_000004.10:g.77161701T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306602.3:c.*406A>G (CXCL10) MANE Select	ENSP00000305651.1:n.*406A>G
ENST00000306602.2:c.*406A>G (CXCL10)	ENSP00000305651.1:n.*406A>G
ENST00000341029.9:c.-10+10204T>C (ART3)	ENSP00000343843.5:n.-10+10204T>C
ENST00000504914.5:c.-10+9281T>C (ART3)	ENSP00000421431.1:n.-10+9281T>C
ENST00000510669.5:n.121+10204T>C (ART3)
ENST00000513122.5:c.-125+10204T>C (ART3)	ENSP00000422287.1:n.-125+10204T>C
ENST00000513353.5:c.-44+10204T>C (ART3)	ENSP00000421345.1:n.-44+10204T>C
NM_001130017.2:c.-10+10204T>C (ART3)	NP_001123489.1:n.-10+10204T>C
NM_001565.3:c.*406A>G (CXCL10)	NP_001556.2:n.*406A>G
XM_017008206.2:c.-44+10204T>C (ART3)	XP_016863695.1:n.-44+10204T>C
XM_024454051.1:c.-10+10204T>C (ART3)	XP_024309819.1:n.-10+10204T>C
XM_024454052.1:c.-125+10204T>C (ART3)	XP_024309820.1:n.-125+10204T>C
XM_024454053.1:c.-136+10204T>C (ART3)	XP_024309821.1:n.-136+10204T>C
XM_024454063.1:c.-10+10204T>C (ART3)	XP_024309831.1:n.-10+10204T>C
NM_001565.4:c.*406A>G (CXCL10) MANE Select	NP_001556.2:n.*406A>G
NM_001130017.3:c.-10+10204T>C (ART3)	NP_001123489.1:n.-10+10204T>C
NM_001377177.1:c.-10+10204T>C (ART3)	NP_001364106.1:n.-10+10204T>C
NM_001377181.1:c.-10+10204T>C (ART3)	NP_001364110.1:n.-10+10204T>C
NM_001377183.1:c.-10+10204T>C (ART3)	NP_001364112.1:n.-10+10204T>C
NR_168520.1:n.642A>G (CXCL10)