Canonical Allele Identifier: CA15523201
Gene: IL6 HGNC NCBI

Linked Data

dbSNP Id: rs2069840
gnomAD v2: 7-22768572-C-G
gnomAD v3: 7-22728953-C-G
gnomAD v4: 7-22728953-C-G
MyVariant Identifiers: chr7:g.22768572C>G (hg19) chr7:g.22728953C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22728953C>G , CM000669.2:g.22728953C>G GRCh38
NC_000007.13:g.22768572C>G , CM000669.1:g.22768572C>G GRCh37
NC_000007.12:g.22735097C>G NCBI36
NG_011640.1:g.6807C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.1630+147C>G
ENST00000258743.10:c.324+147C>G MANE Select ENSP00000258743.5:n.324+147C>G
ENST00000258743.9:c.324+147C>G ENSP00000258743.5:n.324+147C>G
ENST00000401630.7:c.255+147C>G ENSP00000384928.3:n.255+147C>G
ENST00000401651.5:c.96+147C>G ENSP00000385718.1:n.96+147C>G
ENST00000404625.5:c.324+147C>G ENSP00000385675.1:n.324+147C>G
ENST00000406575.1:c.324+147C>G ENSP00000385227.1:n.324+147C>G
ENST00000407492.5:c.96+147C>G ENSP00000385043.1:n.96+147C>G
ENST00000426291.5:c.324+147C>G ENSP00000405150.1:n.324+147C>G
ENST00000464710.1:n.307+147C>G
ENST00000485300.1:n.549+147C>G
NM_000600.3:c.324+147C>G NP_000591.1:n.324+147C>G
XM_005249745.3:c.486+147C>G XP_005249802.1:n.486+147C>G
XM_011515390.1:c.324+147C>G XP_011513692.1:n.324+147C>G
XM_011515391.1:c.96+147C>G XP_011513693.1:n.96+147C>G
NM_000600.4:c.324+147C>G NP_000591.1:n.324+147C>G
NM_001318095.1:c.96+147C>G NP_001305024.1:n.96+147C>G
XM_005249745.5:c.486+147C>G XP_005249802.1:n.486+147C>G
XM_011515390.2:c.324+147C>G XP_011513692.1:n.324+147C>G
NM_000600.5:c.324+147C>G MANE Select NP_000591.1:n.324+147C>G
NM_001318095.2:c.96+147C>G NP_001305024.1:n.96+147C>G
NM_001371096.1:c.255+147C>G NP_001358025.1:n.255+147C>G
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