Canonical Allele Identifier: CA1595020071

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159326937_159326941delinsCCTTT , CM000667.2:g.159326937_159326941delinsCCTTT	GRCh38
NC_000005.9:g.158753945_158753949delinsCCTTT , CM000667.1:g.158753945_158753949delinsCCTTT	GRCh37
NC_000005.8:g.158686523_158686527delinsCCTTT	NCBI36
NG_009618.1:g.8533_8537delinsAAAGG , LRG_71:g.8533_8537delinsAAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+3491_-149+3495delinsAAAGG	ENSP00000512849.1:n.-149+3491_-149+3495delinsAAAGG
ENST00000696751.1:c.1-159_1-155delinsAAAGG	ENSP00000512850.1:n.1-159_1-155delinsAAAGG
ENST00000696752.1:n.433-159_433-155delinsAAAGG
ENST00000231228.3:c.1-159_1-155delinsAAAGG MANE Select	ENSP00000231228.2:n.1-159_1-155delinsAAAGG
ENST00000231228.2:c.1-159_1-155delinsAAAGG	ENSP00000231228.2:n.1-159_1-155delinsAAAGG
NM_002187.2:c.1-159_1-155delinsAAAGG , LRG_71t1:c.1-159_1-155delinsAAAGG	NP_002178.2:n.1-159_1-155delinsAAAGG
NM_002187.3:c.1-159_1-155delinsAAAGG MANE Select	NP_002178.2:n.1-159_1-155delinsAAAGG