Canonical Allele Identifier: CA344482034

Gene: IL10 IL19

Linked Data

• ClinVar Variation Id: 1525940
• ClinVar RCV Id: RCV002037063
• dbSNP Id: rs1307541646
• gnomAD v4: 1-206770962-T-C
• MyVariant Identifiers: chr1:g.206944307T>C (hg19) ; chr1:g.206770962T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770962T>C , CM000663.2:g.206770962T>C	GRCh38
NC_000001.10:g.206944307T>C , CM000663.1:g.206944307T>C	GRCh37
NC_000001.9:g.205010930T>C	NCBI36
NG_012088.1:g.6533A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.228A>G (IL10)
ENST00000471071.2:c.68A>G (IL10)	ENSP00000493073.2:p.His23Arg
ENST00000659065.2:c.206A>G (IL10)	ENSP00000499588.1:p.His69Arg
ENST00000659642.2:c.206A>G (IL10)	ENSP00000499509.1:p.His69Arg
ENST00000664374.2:c.206A>G (IL10)	ENSP00000499664.1:p.His69Arg
ENST00000659997.3:c.-265T>C (IL19) MANE Select	ENSP00000499459.2:n.-265T>C
ENST00000656872.2:c.-149+132T>C (IL19)	ENSP00000499487.2:n.-149+132T>C
ENST00000659065.1:c.206A>G (IL10)	ENSP00000499588.1:p.His69Arg
ENST00000659642.1:c.206A>G (IL10)	ENSP00000499509.1:p.His69Arg
ENST00000659997.2:c.-265T>C (IL19)	ENSP00000499459.2:n.-265T>C
ENST00000662320.1:n.67+132T>C (IL19)
ENST00000664374.1:c.206A>G (IL10)	ENSP00000499664.1:p.His69Arg
ENST00000367099.3:n.228A>G (IL10)
ENST00000423557.1:c.323A>G (IL10) MANE Select	ENSP00000412237.1:p.His108Arg
ENST00000471071.1:n.238A>G (IL10)
NM_000572.2:c.323A>G (IL10)	NP_000563.1:p.His108Arg
XM_011509506.1:c.323A>G (IL10)	XP_011507808.1:p.His108Arg
NM_000572.3:c.323A>G (IL10) MANE Select	NP_000563.1:p.His108Arg
NM_153758.3:c.-151T>C (IL19)	NP_715639.1:n.-151T>C
NM_001382624.1:c.68A>G (IL10)	NP_001369553.1:p.His23Arg
NM_001393490.1:c.-149+132T>C (IL19)	NP_001380419.1:n.-149+132T>C
NM_153758.5:c.-265T>C (IL19) MANE Select	NP_715639.2:n.-265T>C
NR_168466.1:n.382A>G (IL10)