Canonical Allele Identifier: CA36547964

Gene: IL10

Linked Data

• dbSNP Id: rs952013365
• gnomAD v3: 1-206768840-C-G
• gnomAD v4: 1-206768840-C-G
• MyVariant Identifiers: chr1:g.206768840C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768840C>G , CM000663.2:g.206768840C>G	GRCh38
NC_000001.10:g.206942185C>G , CM000663.1:g.206942185C>G	GRCh37
NC_000001.9:g.205008808C>G	NCBI36
NG_012088.1:g.8655G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1338G>C
ENST00000471071.2:c.190-112G>C	ENSP00000493073.2:n.190-112G>C
ENST00000640756.2:n.255-112G>C
ENST00000659065.2:c.328-112G>C	ENSP00000499588.1:n.328-112G>C
ENST00000659642.2:c.328-112G>C	ENSP00000499509.1:n.328-112G>C
ENST00000664374.2:c.328-112G>C	ENSP00000499664.1:n.328-112G>C
ENST00000640756.1:n.244-112G>C
ENST00000659065.1:c.328-112G>C	ENSP00000499588.1:n.328-112G>C
ENST00000659642.1:c.328-112G>C	ENSP00000499509.1:n.328-112G>C
ENST00000664374.1:c.328-112G>C	ENSP00000499664.1:n.328-112G>C
ENST00000423557.1:c.445-112G>C MANE Select	ENSP00000412237.1:n.445-112G>C
ENST00000471071.1:n.360-112G>C
NM_000572.2:c.445-112G>C	NP_000563.1:n.445-112G>C
XM_011509506.1:c.445-112G>C	XP_011507808.1:n.445-112G>C
NM_000572.3:c.445-112G>C MANE Select	NP_000563.1:n.445-112G>C
NM_001382624.1:c.190-112G>C	NP_001369553.1:n.190-112G>C
NR_168466.1:n.742-112G>C
NR_168467.1:n.272-112G>C