Canonical Allele Identifier: CA806427375

Gene: IL12B

Linked Data

• dbSNP Id: rs1287211414
• gnomAD v3: 5-159315048-C-G
• gnomAD v4: 5-159315048-C-G
• MyVariant Identifiers: chr5:g.158742056C>G (hg19) ; chr5:g.159315048C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159315048C>G , CM000667.2:g.159315048C>G	GRCh38
NC_000005.9:g.158742056C>G , CM000667.1:g.158742056C>G	GRCh37
NC_000005.8:g.158674634C>G	NCBI36
NG_009618.1:g.20426G>C , LRG_71:g.20426G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1053G>C	ENSP00000512849.1:n.*1053G>C
ENST00000696751.1:c.*1535G>C	ENSP00000512850.1:n.*1535G>C
ENST00000231228.3:c.*1053G>C MANE Select	ENSP00000231228.2:n.*1053G>C
ENST00000231228.2:c.*1053G>C	ENSP00000231228.2:n.*1053G>C
NM_002187.2:c.*1053G>C , LRG_71t1:c.*1053G>C	NP_002178.2:n.*1053G>C
XR_941138.1:n.364-170C>G
XR_941138.2:n.431-170C>G
NM_002187.3:c.*1053G>C MANE Select	NP_002178.2:n.*1053G>C