Canonical Allele Identifier: CA1595020275

Gene: IL12B

Linked Data

• dbSNP Id: rs3212219

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327453C>T , CM000667.2:g.159327453C>T	GRCh38
NC_000005.9:g.158754461C>T , CM000667.1:g.158754461C>T	GRCh37
NC_000005.8:g.158687039C>T	NCBI36
NG_009618.1:g.8021G>A , LRG_71:g.8021G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+2979G>A	ENSP00000512849.1:n.-149+2979G>A
ENST00000696751.1:c.1-671G>A	ENSP00000512850.1:n.1-671G>A
ENST00000696752.1:n.433-671G>A
ENST00000231228.3:c.1-671G>A MANE Select	ENSP00000231228.2:n.1-671G>A
ENST00000231228.2:c.1-671G>A	ENSP00000231228.2:n.1-671G>A
NM_002187.2:c.1-671G>A , LRG_71t1:c.1-671G>A	NP_002178.2:n.1-671G>A
NM_002187.3:c.1-671G>A MANE Select	NP_002178.2:n.1-671G>A