Canonical Allele Identifier: CA528574386

Gene: IL10

Linked Data

• dbSNP Id: rs1248849279
• gnomAD v2: 1-206942359-T-G
• gnomAD v3: 1-206769014-T-G
• gnomAD v4: 1-206769014-T-G
• MyVariant Identifiers: chr1:g.206942359T>G (hg19) ; chr1:g.206769014T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769014T>G , CM000663.2:g.206769014T>G	GRCh38
NC_000001.10:g.206942359T>G , CM000663.1:g.206942359T>G	GRCh37
NC_000001.9:g.205008982T>G	NCBI36
NG_012088.1:g.8481A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1164A>C
ENST00000471071.2:c.190-286A>C	ENSP00000493073.2:n.190-286A>C
ENST00000640756.2:n.255-286A>C
ENST00000659065.2:c.328-286A>C	ENSP00000499588.1:n.328-286A>C
ENST00000659642.2:c.328-286A>C	ENSP00000499509.1:n.328-286A>C
ENST00000664374.2:c.328-286A>C	ENSP00000499664.1:n.328-286A>C
ENST00000640756.1:n.244-286A>C
ENST00000659065.1:c.328-286A>C	ENSP00000499588.1:n.328-286A>C
ENST00000659642.1:c.328-286A>C	ENSP00000499509.1:n.328-286A>C
ENST00000664374.1:c.328-286A>C	ENSP00000499664.1:n.328-286A>C
ENST00000423557.1:c.445-286A>C MANE Select	ENSP00000412237.1:n.445-286A>C
ENST00000471071.1:n.360-286A>C
NM_000572.2:c.445-286A>C	NP_000563.1:n.445-286A>C
XM_011509506.1:c.445-286A>C	XP_011507808.1:n.445-286A>C
NM_000572.3:c.445-286A>C MANE Select	NP_000563.1:n.445-286A>C
NM_001382624.1:c.190-286A>C	NP_001369553.1:n.190-286A>C
NR_168466.1:n.742-286A>C
NR_168467.1:n.272-286A>C