Canonical Allele Identifier: CA806395136

Gene: IL12B

Linked Data

• dbSNP Id: rs1029383857
• gnomAD v3: 5-159327317-T-G
• gnomAD v4: 5-159327317-T-G
• MyVariant Identifiers: chr5:g.158754325T>G (hg19) ; chr5:g.159327317T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327317T>G , CM000667.2:g.159327317T>G	GRCh38
NC_000005.9:g.158754325T>G , CM000667.1:g.158754325T>G	GRCh37
NC_000005.8:g.158686903T>G	NCBI36
NG_009618.1:g.8157A>C , LRG_71:g.8157A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+3115A>C	ENSP00000512849.1:n.-149+3115A>C
ENST00000696751.1:c.1-535A>C	ENSP00000512850.1:n.1-535A>C
ENST00000696752.1:n.433-535A>C
ENST00000231228.3:c.1-535A>C MANE Select	ENSP00000231228.2:n.1-535A>C
ENST00000231228.2:c.1-535A>C	ENSP00000231228.2:n.1-535A>C
NM_002187.2:c.1-535A>C , LRG_71t1:c.1-535A>C	NP_002178.2:n.1-535A>C
NM_002187.3:c.1-535A>C MANE Select	NP_002178.2:n.1-535A>C