Canonical Allele Identifier: CA1595018047

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322053_159322054delinsCA , CM000667.2:g.159322053_159322054delinsCA	GRCh38
NC_000005.9:g.158749061_158749062delinsCA , CM000667.1:g.158749061_158749062delinsCA	GRCh37
NC_000005.8:g.158681639_158681640delinsCA	NCBI36
NG_009618.1:g.13420_13421delinsTG , LRG_71:g.13420_13421delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1534_-148-1533delinsTG	ENSP00000512849.1:n.-148-1534_-148-1533delinsTG
ENST00000696751.1:c.364+1000_364+1001delinsTG	ENSP00000512850.1:n.364+1000_364+1001delinsTG
ENST00000231228.3:c.482+340_482+341delinsTG MANE Select	ENSP00000231228.2:n.482+340_482+341delinsTG
ENST00000231228.2:c.482+340_482+341delinsTG	ENSP00000231228.2:n.482+340_482+341delinsTG
NM_002187.2:c.482+340_482+341delinsTG , LRG_71t1:c.482+340_482+341delinsTG	NP_002178.2:n.482+340_482+341delinsTG
XR_001742945.1:n.147+1457_147+1458delinsCA
NM_002187.3:c.482+340_482+341delinsTG MANE Select	NP_002178.2:n.482+340_482+341delinsTG