Canonical Allele Identifier: CA36549107

Gene: IL10

Linked Data

• dbSNP Id: rs574072199
• gnomAD v3: 1-206770746-G-C
• gnomAD v4: 1-206770746-G-C
• MyVariant Identifiers: chr1:g.206944091G>C (hg19) ; chr1:g.206770746G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770746G>C , CM000663.2:g.206770746G>C	GRCh38
NC_000001.10:g.206944091G>C , CM000663.1:g.206944091G>C	GRCh37
NC_000001.9:g.205010714G>C	NCBI36
NG_012088.1:g.6749C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+161C>G
ENST00000471071.2:c.123+161C>G	ENSP00000493073.2:n.123+161C>G
ENST00000659065.2:c.261+161C>G	ENSP00000499588.1:n.261+161C>G
ENST00000659642.2:c.261+161C>G	ENSP00000499509.1:n.261+161C>G
ENST00000664374.2:c.261+161C>G	ENSP00000499664.1:n.261+161C>G
ENST00000659065.1:c.261+161C>G	ENSP00000499588.1:n.261+161C>G
ENST00000659642.1:c.261+161C>G	ENSP00000499509.1:n.261+161C>G
ENST00000664374.1:c.261+161C>G	ENSP00000499664.1:n.261+161C>G
ENST00000367099.3:n.283+161C>G
ENST00000423557.1:c.378+161C>G MANE Select	ENSP00000412237.1:n.378+161C>G
ENST00000471071.1:n.293+161C>G
NM_000572.2:c.378+161C>G	NP_000563.1:n.378+161C>G
XM_011509506.1:c.378+161C>G	XP_011507808.1:n.378+161C>G
NM_000572.3:c.378+161C>G MANE Select	NP_000563.1:n.378+161C>G
NM_001382624.1:c.123+161C>G	NP_001369553.1:n.123+161C>G
NR_168466.1:n.437+161C>G