Canonical Allele Identifier: CA15500966
Gene: IL6 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.22728408A>G
GRCh37 chr7:g.22768027A>G
gnomAD v2:
7:22768027 A / G
gnomAD v3:
7:22728408 A / G
gnomAD v4:
chr7-22728408-A-G
Joint Max Group AF 0.15879975 (EAS)
Genomes Max Group AF 0.16076278 (EAS)
Exomes Max Group AF 0.15609454 (EAS)
dbSNP:
2069837
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22728408A>G , CM000669.2:g.22728408A>G GRCh38
NC_000007.13:g.22768027A>G , CM000669.1:g.22768027A>G GRCh37
NC_000007.12:g.22734552A>G NCBI36
NG_011640.1:g.6262A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000464710.2:n.1232A>G
ENST00000258743.10:c.211-285A>G MANE Select ENSP00000258743.5:n.211-285A>G
ENST00000258743.9:c.211-285A>G ENSP00000258743.5:n.211-285A>G
ENST00000401630.7:c.142-285A>G ENSP00000384928.3:n.142-285A>G
ENST00000401651.5:c.-18-285A>G ENSP00000385718.1:n.-18-285A>G
ENST00000404625.5:c.211-285A>G ENSP00000385675.1:n.211-285A>G
ENST00000406575.1:c.211-285A>G ENSP00000385227.1:n.211-285A>G
ENST00000407492.5:c.-18-285A>G ENSP00000385043.1:n.-18-285A>G
ENST00000426291.5:c.211-285A>G ENSP00000405150.1:n.211-285A>G
ENST00000485300.1:n.436-285A>G
NM_000600.3:c.211-285A>G NP_000591.1:n.211-285A>G
XM_005249745.3:c.373-285A>G XP_005249802.1:n.373-285A>G
XM_011515390.1:c.211-285A>G XP_011513692.1:n.211-285A>G
XM_011515391.1:c.-18-285A>G XP_011513693.1:n.-18-285A>G
NM_000600.4:c.211-285A>G NP_000591.1:n.211-285A>G
NM_001318095.1:c.-18-285A>G NP_001305024.1:n.-18-285A>G
XM_005249745.5:c.373-285A>G XP_005249802.1:n.373-285A>G
XM_011515390.2:c.211-285A>G XP_011513692.1:n.211-285A>G
NM_000600.5:c.211-285A>G MANE Select NP_000591.1:n.211-285A>G
NM_001318095.2:c.-18-285A>G NP_001305024.1:n.-18-285A>G
NM_001371096.1:c.142-285A>G NP_001358025.1:n.142-285A>G
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