Canonical Allele Identifier: CA1837283
Gene: IL1B HGNC NCBI

Linked Data

dbSNP Id: rs751922568
ExAC: 2:113590198 G / T
gnomAD v2: 2-113590198-G-T
gnomAD v3: 2-112832621-G-T
gnomAD v4: 2-112832621-G-T
MyVariant Identifiers: chr2:g.113590198G>T (hg19) chr2:g.112832621G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112832621G>T , CM000664.2:g.112832621G>T GRCh38
NC_000002.11:g.113590198G>T , CM000664.1:g.113590198G>T GRCh37
NC_000002.10:g.113306669G>T NCBI36
NG_008851.1:g.9159C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263341.7:c.466+41C>A MANE Select ENSP00000263341.2:n.466+41C>A
ENST00000263341.6:c.466+41C>A ENSP00000263341.2:n.466+41C>A
ENST00000487639.1:n.367+41C>A
ENST00000491056.5:n.1273+41C>A
NM_000576.2:c.466+41C>A NP_000567.1:n.466+41C>A
XM_006712496.1:c.232+41C>A XP_006712559.1:n.232+41C>A
XM_017003988.2:c.373+41C>A XP_016859477.1:n.373+41C>A
NM_000576.3:c.466+41C>A MANE Select NP_000567.1:n.466+41C>A
Search 100 bp 5'
Search 100 bp 3'