Canonical Allele Identifier: CA806428117

Gene: IL12B

Linked Data

• dbSNP Id: rs1279252037
• gnomAD v3: 5-159316206-A-G
• gnomAD v4: 5-159316206-A-G
• MyVariant Identifiers: chr5:g.158743214A>G (hg19) ; chr5:g.159316206A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316206A>G , CM000667.2:g.159316206A>G	GRCh38
NC_000005.9:g.158743214A>G , CM000667.1:g.158743214A>G	GRCh37
NC_000005.8:g.158675792A>G	NCBI36
NG_009618.1:g.19268T>C , LRG_71:g.19268T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*1-106T>C	ENSP00000512849.1:n.*1-106T>C
ENST00000696751.1:c.*483-106T>C	ENSP00000512850.1:n.*483-106T>C
ENST00000231228.3:c.*1-106T>C MANE Select	ENSP00000231228.2:n.*1-106T>C
ENST00000231228.2:c.*1-106T>C	ENSP00000231228.2:n.*1-106T>C
NM_002187.2:c.*1-106T>C , LRG_71t1:c.*1-106T>C	NP_002178.2:n.*1-106T>C
NM_002187.3:c.*1-106T>C MANE Select	NP_002178.2:n.*1-106T>C