Canonical Allele Identifier: CA2483126868

Linked Data

dbSNP Id: rs1674848041

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771655G>C , CM000663.2:g.206771655G>C GRCh38
NC_000001.10:g.206945000G>C , CM000663.1:g.206945000G>C GRCh37
NC_000001.9:g.205011623G>C NCBI36
NG_012088.1:g.5840C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.49-240C>G (IL10) ENSP00000499588.1:n.49-240C>G
ENST00000659642.2:c.49-240C>G (IL10) ENSP00000499509.1:n.49-240C>G
ENST00000664374.2:c.49-240C>G (IL10) ENSP00000499664.1:n.49-240C>G
ENST00000659997.3:c.-149+577G>C (IL19) MANE Select ENSP00000499459.2:n.-149+577G>C
ENST00000656872.2:c.-149+825G>C (IL19) ENSP00000499487.2:n.-149+825G>C
ENST00000659065.1:c.49-240C>G (IL10) ENSP00000499588.1:n.49-240C>G
ENST00000659642.1:c.49-240C>G (IL10) ENSP00000499509.1:n.49-240C>G
ENST00000659997.2:c.-149+577G>C (IL19) ENSP00000499459.2:n.-149+577G>C
ENST00000662320.1:n.67+825G>C (IL19)
ENST00000664374.1:c.49-240C>G (IL10) ENSP00000499664.1:n.49-240C>G
ENST00000423557.1:c.166-240C>G (IL10) MANE Select ENSP00000412237.1:n.166-240C>G
NM_000572.2:c.166-240C>G (IL10) NP_000563.1:n.166-240C>G
XM_011509506.1:c.166-240C>G (IL10) XP_011507808.1:n.166-240C>G
NM_000572.3:c.166-240C>G (IL10) MANE Select NP_000563.1:n.166-240C>G
NM_153758.3:c.-35+577G>C (IL19) NP_715639.1:n.-35+577G>C
NM_001393490.1:c.-149+825G>C (IL19) NP_001380419.1:n.-149+825G>C
NM_153758.5:c.-149+577G>C (IL19) MANE Select NP_715639.2:n.-149+577G>C
NR_168466.1:n.225-240C>G (IL10)