Canonical Allele Identifier: CA1595020734

Gene: IL12B

Linked Data

• dbSNP Id: rs1003199

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328558C>A , CM000667.2:g.159328558C>A	GRCh38
NC_000005.9:g.158755566C>A , CM000667.1:g.158755566C>A	GRCh37
NC_000005.8:g.158688144C>A	NCBI36
NG_009618.1:g.6916G>T , LRG_71:g.6916G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1874G>T	ENSP00000512849.1:n.-149+1874G>T
ENST00000696751.1:c.1-1776G>T	ENSP00000512850.1:n.1-1776G>T
ENST00000696752.1:n.433-1776G>T
ENST00000231228.3:c.1-1776G>T MANE Select	ENSP00000231228.2:n.1-1776G>T
ENST00000231228.2:c.1-1776G>T	ENSP00000231228.2:n.1-1776G>T
NM_002187.2:c.1-1776G>T , LRG_71t1:c.1-1776G>T	NP_002178.2:n.1-1776G>T
NM_002187.3:c.1-1776G>T MANE Select	NP_002178.2:n.1-1776G>T