Canonical Allele Identifier: CA129826952

Gene: IL12B

Linked Data

• dbSNP Id: rs56369079
• gnomAD v4: 5-159320519-A-G
• MyVariant Identifiers: chr5:g.158747527A>G (hg19) ; chr5:g.159320519A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320519A>G , CM000667.2:g.159320519A>G	GRCh38
NC_000005.9:g.158747527A>G , CM000667.1:g.158747527A>G	GRCh37
NC_000005.8:g.158680105A>G	NCBI36
NG_009618.1:g.14955T>C , LRG_71:g.14955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-147T>C	ENSP00000512849.1:n.-147T>C
ENST00000696751.1:c.366T>C	ENSP00000512850.1:p.Ala122=
ENST00000231228.3:c.484T>C MANE Select	ENSP00000231228.2:p.Ser162Pro
ENST00000231228.2:c.484T>C	ENSP00000231228.2:p.Ser162Pro
NM_002187.2:c.484T>C , LRG_71t1:c.484T>C	NP_002178.2:p.Ser162Pro
XR_001742945.1:n.70A>G
NM_002187.3:c.484T>C MANE Select	NP_002178.2:p.Ser162Pro