Canonical Allele Identifier: CA1083491169

Gene: IL12B

Linked Data

• dbSNP Id: rs1754232315
• gnomAD v3: 5-159328828-T-A
• gnomAD v4: 5-159328828-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328828T>A , CM000667.2:g.159328828T>A	GRCh38
NC_000005.9:g.158755836T>A , CM000667.1:g.158755836T>A	GRCh37
NC_000005.8:g.158688414T>A	NCBI36
NG_009618.1:g.6646A>T , LRG_71:g.6646A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1604A>T	ENSP00000512849.1:n.-149+1604A>T
ENST00000696751.1:c.-1+1604A>T	ENSP00000512850.1:n.-1+1604A>T
ENST00000696752.1:n.432+1604A>T
ENST00000231228.3:c.-1+1604A>T MANE Select	ENSP00000231228.2:n.-1+1604A>T
ENST00000231228.2:c.-1+1604A>T	ENSP00000231228.2:n.-1+1604A>T
NM_002187.2:c.-1+1604A>T , LRG_71t1:c.-1+1604A>T	NP_002178.2:n.-1+1604A>T
NM_002187.3:c.-1+1604A>T MANE Select	NP_002178.2:n.-1+1604A>T