Canonical Allele Identifier: CA362032552

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747380T>G (hg19) ; chr5:g.159320372T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320372T>G , CM000667.2:g.159320372T>G	GRCh38
NC_000005.9:g.158747380T>G , CM000667.1:g.158747380T>G	GRCh37
NC_000005.8:g.158679958T>G	NCBI36
NG_009618.1:g.15102A>C , LRG_71:g.15102A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.1A>C	ENSP00000512849.1:p.Met1Leu
ENST00000696751.1:c.*126A>C	ENSP00000512850.1:n.*126A>C
ENST00000231228.3:c.631A>C MANE Select	ENSP00000231228.2:p.Met211Leu
ENST00000231228.2:c.631A>C	ENSP00000231228.2:p.Met211Leu
NM_002187.2:c.631A>C , LRG_71t1:c.631A>C	NP_002178.2:p.Met211Leu
NM_002187.3:c.631A>C MANE Select	NP_002178.2:p.Met211Leu