Canonical Allele Identifier: CA10699290

Linked Data

ClinVar Variation Id: 16873
dbSNP Id: rs1800872

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773062T>G , CM000663.2:g.206773062T>G GRCh38
NC_000001.10:g.206946407T>G , CM000663.1:g.206946407T>G GRCh37
NC_000001.9:g.205013030T>G NCBI36
NG_012088.1:g.4433A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.-15+618A>C (IL10) ENSP00000499588.1:n.-15+618A>C
ENST00000659642.2:c.-744A>C (IL10) ENSP00000499509.1:n.-744A>C
ENST00000664374.2:c.-14-730A>C (IL10) ENSP00000499664.1:n.-14-730A>C
ENST00000659997.3:c.-149+1984T>G (IL19) MANE Select ENSP00000499459.2:n.-149+1984T>G
ENST00000656872.2:c.-149+2232T>G (IL19) ENSP00000499487.2:n.-149+2232T>G
ENST00000659065.1:c.-15+618A>C (IL10) ENSP00000499588.1:n.-15+618A>C
ENST00000659642.1:c.-744A>C (IL10) ENSP00000499509.1:n.-744A>C
ENST00000659997.2:c.-149+1984T>G (IL19) ENSP00000499459.2:n.-149+1984T>G
ENST00000662320.1:n.67+2232T>G (IL19)
ENST00000664374.1:c.-14-730A>C (IL10) ENSP00000499664.1:n.-14-730A>C
XM_011509506.1:c.-627A>C (IL10) XP_011507808.1:n.-627A>C
NM_153758.3:c.-35+1984T>G (IL19) NP_715639.1:n.-35+1984T>G
NM_001393490.1:c.-149+2232T>G (IL19) NP_001380419.1:n.-149+2232T>G
NM_153758.5:c.-149+1984T>G (IL19) MANE Select NP_715639.2:n.-149+1984T>G