Canonical Allele Identifier: CA36551968

Gene: IL10 IL19

Linked Data

• dbSNP Id: rs902509261
• gnomAD v2: 1-206947081-T-C
• gnomAD v3: 1-206773736-T-C
• gnomAD v4: 1-206773736-T-C
• MyVariant Identifiers: chr1:g.206947081T>C (hg19) ; chr1:g.206773736T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206773736T>C , CM000663.2:g.206773736T>C	GRCh38
NC_000001.10:g.206947081T>C , CM000663.1:g.206947081T>C	GRCh37
NC_000001.9:g.205013704T>C	NCBI36
NG_012088.1:g.3759A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000659065.2:c.-71A>G (IL10)	ENSP00000499588.1:n.-71A>G
ENST00000659642.2:c.-1118-300A>G (IL10)	ENSP00000499509.1:n.-1118-300A>G
ENST00000664374.2:c.-15+594A>G (IL10)	ENSP00000499664.1:n.-15+594A>G
ENST00000659997.3:c.-149+2658T>C (IL19) MANE Select	ENSP00000499459.2:n.-149+2658T>C
ENST00000656872.2:c.-149+2906T>C (IL19)	ENSP00000499487.2:n.-149+2906T>C
ENST00000659065.1:c.-71A>G (IL10)	ENSP00000499588.1:n.-71A>G
ENST00000659642.1:c.-1118-300A>G (IL10)	ENSP00000499509.1:n.-1118-300A>G
ENST00000659997.2:c.-149+2658T>C (IL19)	ENSP00000499459.2:n.-149+2658T>C
ENST00000662320.1:n.67+2906T>C (IL19)
ENST00000664374.1:c.-15+594A>G (IL10)	ENSP00000499664.1:n.-15+594A>G
XM_011509506.1:c.-1001-300A>G (IL10)	XP_011507808.1:n.-1001-300A>G
NM_153758.3:c.-35+2658T>C (IL19)	NP_715639.1:n.-35+2658T>C
NM_001393490.1:c.-149+2906T>C (IL19)	NP_001380419.1:n.-149+2906T>C
NM_153758.5:c.-149+2658T>C (IL19) MANE Select	NP_715639.2:n.-149+2658T>C