Canonical Allele Identifier: CA2536164420

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321879_159321880insAT , CM000667.2:g.159321879_159321880insAT	GRCh38
NC_000005.9:g.158748887_158748888insAT , CM000667.1:g.158748887_158748888insAT	GRCh37
NC_000005.8:g.158681465_158681466insAT	NCBI36
NG_009618.1:g.13594_13595insAT , LRG_71:g.13594_13595insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1360_-148-1359insAT	ENSP00000512849.1:n.-148-1360_-148-1359insAT
ENST00000696751.1:c.364+1174_364+1175insAT	ENSP00000512850.1:n.364+1174_364+1175insAT
ENST00000231228.3:c.482+514_482+515insAT MANE Select	ENSP00000231228.2:n.482+514_482+515insAT
ENST00000231228.2:c.482+514_482+515insAT	ENSP00000231228.2:n.482+514_482+515insAT
NM_002187.2:c.482+514_482+515insAT , LRG_71t1:c.482+514_482+515insAT	NP_002178.2:n.482+514_482+515insAT
XR_001742945.1:n.147+1283_147+1284insAT
NM_002187.3:c.482+514_482+515insAT MANE Select	NP_002178.2:n.482+514_482+515insAT