Canonical Allele Identifier: CA422931760

Linked Data

MyVariant Identifiers: chr1:g.206944396C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771051C>A , CM000663.2:g.206771051C>A GRCh38
NC_000001.10:g.206944396C>A , CM000663.1:g.206944396C>A GRCh37
NC_000001.9:g.205011019C>A NCBI36
NG_012088.1:g.6444G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.139G>T (IL10)
ENST00000471071.2:c.-22G>T (IL10) ENSP00000493073.2:n.-22G>T
ENST00000659065.2:c.117G>T (IL10) ENSP00000499588.1:p.Leu39=
ENST00000659642.2:c.117G>T (IL10) ENSP00000499509.1:p.Leu39=
ENST00000664374.2:c.117G>T (IL10) ENSP00000499664.1:p.Leu39=
ENST00000659997.3:c.-176C>A (IL19) MANE Select ENSP00000499459.2:n.-176C>A
ENST00000656872.2:c.-149+221C>A (IL19) ENSP00000499487.2:n.-149+221C>A
ENST00000659065.1:c.117G>T (IL10) ENSP00000499588.1:p.Leu39=
ENST00000659642.1:c.117G>T (IL10) ENSP00000499509.1:p.Leu39=
ENST00000659997.2:c.-176C>A (IL19) ENSP00000499459.2:n.-176C>A
ENST00000662320.1:n.67+221C>A (IL19)
ENST00000664374.1:c.117G>T (IL10) ENSP00000499664.1:p.Leu39=
ENST00000367099.3:n.139G>T (IL10)
ENST00000423557.1:c.234G>T (IL10) MANE Select ENSP00000412237.1:p.Leu78=
ENST00000471071.1:n.149G>T (IL10)
NM_000572.2:c.234G>T (IL10) NP_000563.1:p.Leu78=
XM_011509506.1:c.234G>T (IL10) XP_011507808.1:p.Leu78=
NM_000572.3:c.234G>T (IL10) MANE Select NP_000563.1:p.Leu78=
NM_153758.3:c.-62C>A (IL19) NP_715639.1:n.-62C>A
NM_001382624.1:c.-22G>T (IL10) NP_001369553.1:n.-22G>T
NM_001393490.1:c.-149+221C>A (IL19) NP_001380419.1:n.-149+221C>A
NM_153758.5:c.-176C>A (IL19) MANE Select NP_715639.2:n.-176C>A
NR_168466.1:n.293G>T (IL10)