Canonical Allele Identifier: CA806428090

Gene: IL12B

Linked Data

• dbSNP Id: rs1464173330
• MyVariant Identifiers: chr5:g.158743168A>C (hg19) ; chr5:g.159316160A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316160A>C , CM000667.2:g.159316160A>C	GRCh38
NC_000005.9:g.158743168A>C , CM000667.1:g.158743168A>C	GRCh37
NC_000005.8:g.158675746A>C	NCBI36
NG_009618.1:g.19314T>G , LRG_71:g.19314T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*1-60T>G	ENSP00000512849.1:n.*1-60T>G
ENST00000696751.1:c.*483-60T>G	ENSP00000512850.1:n.*483-60T>G
ENST00000231228.3:c.*1-60T>G MANE Select	ENSP00000231228.2:n.*1-60T>G
ENST00000231228.2:c.*1-60T>G	ENSP00000231228.2:n.*1-60T>G
NM_002187.2:c.*1-60T>G , LRG_71t1:c.*1-60T>G	NP_002178.2:n.*1-60T>G
NM_002187.3:c.*1-60T>G MANE Select	NP_002178.2:n.*1-60T>G