Canonical Allele Identifier: CA806394943

Gene: IL12B

Linked Data

• dbSNP Id: rs1479811009
• gnomAD v3: 5-159326997-T-A
• gnomAD v4: 5-159326997-T-A
• MyVariant Identifiers: chr5:g.158754005T>A (hg19) ; chr5:g.159326997T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159326997T>A , CM000667.2:g.159326997T>A	GRCh38
NC_000005.9:g.158754005T>A , CM000667.1:g.158754005T>A	GRCh37
NC_000005.8:g.158686583T>A	NCBI36
NG_009618.1:g.8477A>T , LRG_71:g.8477A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+3435A>T	ENSP00000512849.1:n.-149+3435A>T
ENST00000696751.1:c.1-215A>T	ENSP00000512850.1:n.1-215A>T
ENST00000696752.1:n.433-215A>T
ENST00000231228.3:c.1-215A>T MANE Select	ENSP00000231228.2:n.1-215A>T
ENST00000231228.2:c.1-215A>T	ENSP00000231228.2:n.1-215A>T
NM_002187.2:c.1-215A>T , LRG_71t1:c.1-215A>T	NP_002178.2:n.1-215A>T
NM_002187.3:c.1-215A>T MANE Select	NP_002178.2:n.1-215A>T