Canonical Allele Identifier: CA344482006

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206770948C>A , CM000663.2:g.206770948C>A GRCh38
NC_000001.10:g.206944293C>A , CM000663.1:g.206944293C>A GRCh37
NC_000001.9:g.205010916C>A NCBI36
NG_012088.1:g.6547G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.242G>T (IL10)
ENST00000471071.2:c.82G>T (IL10) ENSP00000493073.2:p.Gly28Trp
ENST00000659065.2:c.220G>T (IL10) ENSP00000499588.1:p.Gly74Trp
ENST00000659642.2:c.220G>T (IL10) ENSP00000499509.1:p.Gly74Trp
ENST00000664374.2:c.220G>T (IL10) ENSP00000499664.1:p.Gly74Trp
ENST00000659997.3:c.-279C>A (IL19) MANE Select ENSP00000499459.2:n.-279C>A
ENST00000656872.2:c.-149+118C>A (IL19) ENSP00000499487.2:n.-149+118C>A
ENST00000659065.1:c.220G>T (IL10) ENSP00000499588.1:p.Gly74Trp
ENST00000659642.1:c.220G>T (IL10) ENSP00000499509.1:p.Gly74Trp
ENST00000659997.2:c.-279C>A (IL19) ENSP00000499459.2:n.-279C>A
ENST00000662320.1:n.67+118C>A (IL19)
ENST00000664374.1:c.220G>T (IL10) ENSP00000499664.1:p.Gly74Trp
ENST00000367099.3:n.242G>T (IL10)
ENST00000423557.1:c.337G>T (IL10) MANE Select ENSP00000412237.1:p.Gly113Trp
ENST00000471071.1:n.252G>T (IL10)
NM_000572.2:c.337G>T (IL10) NP_000563.1:p.Gly113Trp
XM_011509506.1:c.337G>T (IL10) XP_011507808.1:p.Gly113Trp
NM_000572.3:c.337G>T (IL10) MANE Select NP_000563.1:p.Gly113Trp
NM_153758.3:c.-165C>A (IL19) NP_715639.1:n.-165C>A
NM_001382624.1:c.82G>T (IL10) NP_001369553.1:p.Gly28Trp
NM_001393490.1:c.-149+118C>A (IL19) NP_001380419.1:n.-149+118C>A
NM_153758.5:c.-279C>A (IL19) MANE Select NP_715639.2:n.-279C>A
NR_168466.1:n.396G>T (IL10)