Canonical Allele Identifier: CA348288472

Gene: IL1B

Linked Data

• MyVariant Identifiers: chr2:g.113590404C>A (hg19) ; chr2:g.112832827C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112832827C>A , CM000664.2:g.112832827C>A	GRCh38
NC_000002.11:g.113590404C>A , CM000664.1:g.113590404C>A	GRCh37
NC_000002.10:g.113306875C>A	NCBI36
NG_008851.1:g.8953G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263341.7:c.302-1G>T MANE Select	ENSP00000263341.2:n.302-1G>T
ENST00000263341.6:c.302-1G>T	ENSP00000263341.2:n.302-1G>T
ENST00000416750.1:c.302-1G>T	ENSP00000400854.1:n.302-1G>T
ENST00000418817.5:c.302-1G>T	ENSP00000407219.1:n.302-1G>T
ENST00000432018.5:c.302-1G>T	ENSP00000409680.1:n.302-1G>T
ENST00000487639.1:n.203-1G>T
ENST00000491056.5:n.1109-1G>T
NM_000576.2:c.302-1G>T	NP_000567.1:n.302-1G>T
XM_006712496.1:c.68-1G>T	XP_006712559.1:n.68-1G>T
XM_017003988.2:c.209-1G>T	XP_016859477.1:n.209-1G>T
NM_000576.3:c.302-1G>T MANE Select	NP_000567.1:n.302-1G>T