Canonical Allele Identifier: CA36547978
Gene: IL10 HGNC NCBI

Linked Data

dbSNP Id: rs976668241

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206768849G>A , CM000663.2:g.206768849G>A GRCh38
NC_000001.10:g.206942194G>A , CM000663.1:g.206942194G>A GRCh37
NC_000001.9:g.205008817G>A NCBI36
NG_012088.1:g.8646C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.1329C>T
ENST00000471071.2:c.190-121C>T ENSP00000493073.2:n.190-121C>T
ENST00000640756.2:n.255-121C>T
ENST00000659065.2:c.328-121C>T ENSP00000499588.1:n.328-121C>T
ENST00000659642.2:c.328-121C>T ENSP00000499509.1:n.328-121C>T
ENST00000664374.2:c.328-121C>T ENSP00000499664.1:n.328-121C>T
ENST00000640756.1:n.244-121C>T
ENST00000659065.1:c.328-121C>T ENSP00000499588.1:n.328-121C>T
ENST00000659642.1:c.328-121C>T ENSP00000499509.1:n.328-121C>T
ENST00000664374.1:c.328-121C>T ENSP00000499664.1:n.328-121C>T
ENST00000423557.1:c.445-121C>T MANE Select ENSP00000412237.1:n.445-121C>T
ENST00000471071.1:n.360-121C>T
NM_000572.2:c.445-121C>T NP_000563.1:n.445-121C>T
XM_011509506.1:c.445-121C>T XP_011507808.1:n.445-121C>T
NM_000572.3:c.445-121C>T MANE Select NP_000563.1:n.445-121C>T
NM_001382624.1:c.190-121C>T NP_001369553.1:n.190-121C>T
NR_168466.1:n.742-121C>T
NR_168467.1:n.272-121C>T