Canonical Allele Identifier: CA1595018073

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322120_159322121delinsTG , CM000667.2:g.159322120_159322121delinsTG	GRCh38
NC_000005.9:g.158749128_158749129delinsTG , CM000667.1:g.158749128_158749129delinsTG	GRCh37
NC_000005.8:g.158681706_158681707delinsTG	NCBI36
NG_009618.1:g.13353_13354delinsCA , LRG_71:g.13353_13354delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-1601_-148-1600delinsCA	ENSP00000512849.1:n.-148-1601_-148-1600de...
ENST00000696751.1:c.364+933_364+934delinsCA	ENSP00000512850.1:n.364+933_364+934delins...
ENST00000231228.3:c.482+273_482+274delinsCA MANE Select	ENSP00000231228.2:n.482+273_482+274delins...
ENST00000231228.2:c.482+273_482+274delinsCA	ENSP00000231228.2:n.482+273_482+274delins...
NM_002187.2:c.482+273_482+274delinsCA , LRG_71t1:c.482+273_482+274delinsCA	NP_002178.2:n.482+273_482+274delinsCA
XR_001742945.1:n.147+1524_147+1525delinsTG
NM_002187.3:c.482+273_482+274delinsCA MANE Select	NP_002178.2:n.482+273_482+274delinsCA