Canonical Allele Identifier: CA806391630

Gene: IL12B

Linked Data

• dbSNP Id: rs1393409906
• gnomAD v3: 5-159322869-T-C
• gnomAD v4: 5-159322869-T-C
• MyVariant Identifiers: chr5:g.158749877T>C (hg19) ; chr5:g.159322869T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322869T>C , CM000667.2:g.159322869T>C	GRCh38
NC_000005.9:g.158749877T>C , CM000667.1:g.158749877T>C	GRCh37
NC_000005.8:g.158682455T>C	NCBI36
NG_009618.1:g.12605A>G , LRG_71:g.12605A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2349A>G	ENSP00000512849.1:n.-148-2349A>G
ENST00000696751.1:c.364+185A>G	ENSP00000512850.1:n.364+185A>G
ENST00000231228.3:c.364+185A>G MANE Select	ENSP00000231228.2:n.364+185A>G
ENST00000231228.2:c.364+185A>G	ENSP00000231228.2:n.364+185A>G
NM_002187.2:c.364+185A>G , LRG_71t1:c.364+185A>G	NP_002178.2:n.364+185A>G
XR_001742945.1:n.147+2273T>C
NM_002187.3:c.364+185A>G MANE Select	NP_002178.2:n.364+185A>G