Canonical Allele Identifier: CA1363780

Gene: IL10 IL19

Linked Data

• ClinVar Variation Id: 1056748
• ClinVar RCV Id: RCV001365626
• dbSNP Id: rs372883095
• ExAC: 1:206944316 A / C
• gnomAD v2: 1-206944316-A-C
• gnomAD v4: 1-206770971-A-C
• MyVariant Identifiers: chr1:g.206944316A>C (hg19) ; chr1:g.206770971A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770971A>C , CM000663.2:g.206770971A>C	GRCh38
NC_000001.10:g.206944316A>C , CM000663.1:g.206944316A>C	GRCh37
NC_000001.9:g.205010939A>C	NCBI36
NG_012088.1:g.6524T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.219T>G (IL10)
ENST00000471071.2:c.59T>G (IL10)	ENSP00000493073.2:p.Ile20Ser
ENST00000659065.2:c.197T>G (IL10)	ENSP00000499588.1:p.Ile66Ser
ENST00000659642.2:c.197T>G (IL10)	ENSP00000499509.1:p.Ile66Ser
ENST00000664374.2:c.197T>G (IL10)	ENSP00000499664.1:p.Ile66Ser
ENST00000659997.3:c.-256A>C (IL19) MANE Select	ENSP00000499459.2:n.-256A>C
ENST00000656872.2:c.-149+141A>C (IL19)	ENSP00000499487.2:n.-149+141A>C
ENST00000659065.1:c.197T>G (IL10)	ENSP00000499588.1:p.Ile66Ser
ENST00000659642.1:c.197T>G (IL10)	ENSP00000499509.1:p.Ile66Ser
ENST00000659997.2:c.-256A>C (IL19)	ENSP00000499459.2:n.-256A>C
ENST00000662320.1:n.67+141A>C (IL19)
ENST00000664374.1:c.197T>G (IL10)	ENSP00000499664.1:p.Ile66Ser
ENST00000367099.3:n.219T>G (IL10)
ENST00000423557.1:c.314T>G (IL10) MANE Select	ENSP00000412237.1:p.Ile105Ser
ENST00000471071.1:n.229T>G (IL10)
NM_000572.2:c.314T>G (IL10)	NP_000563.1:p.Ile105Ser
XM_011509506.1:c.314T>G (IL10)	XP_011507808.1:p.Ile105Ser
NM_000572.3:c.314T>G (IL10) MANE Select	NP_000563.1:p.Ile105Ser
NM_153758.3:c.-142A>C (IL19)	NP_715639.1:n.-142A>C
NM_001382624.1:c.59T>G (IL10)	NP_001369553.1:p.Ile20Ser
NM_001393490.1:c.-149+141A>C (IL19)	NP_001380419.1:n.-149+141A>C
NM_153758.5:c.-256A>C (IL19) MANE Select	NP_715639.2:n.-256A>C
NR_168466.1:n.373T>G (IL10)