Canonical Allele Identifier: CA1595018437
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323009_159323010delinsAT , CM000667.2:g.159323009_159323010delinsAT GRCh38
NC_000005.9:g.158750017_158750018delinsAT , CM000667.1:g.158750017_158750018delinsAT GRCh37
NC_000005.8:g.158682595_158682596delinsAT NCBI36
NG_009618.1:g.12464_12465delinsAT , LRG_71:g.12464_12465delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2490_-148-2489delinsAT ENSP00000512849.1:n.-148-2490_-148-2489de...
ENST00000696751.1:c.364+44_364+45delinsAT ENSP00000512850.1:n.364+44_364+45delinsAT...
ENST00000231228.3:c.364+44_364+45delinsAT MANE Select ENSP00000231228.2:n.364+44_364+45delinsAT...
ENST00000231228.2:c.364+44_364+45delinsAT ENSP00000231228.2:n.364+44_364+45delinsAT...
NM_002187.2:c.364+44_364+45delinsAT , LRG_71t1:c.364+44_364+45delinsAT NP_002178.2:n.364+44_364+45delinsAT
XR_001742945.1:n.147+2413_147+2414delinsAT
NM_002187.3:c.364+44_364+45delinsAT MANE Select NP_002178.2:n.364+44_364+45delinsAT