Canonical Allele Identifier: CA447510880

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747369G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320361G>C , CM000667.2:g.159320361G>C	GRCh38
NC_000005.9:g.158747369G>C , CM000667.1:g.158747369G>C	GRCh37
NC_000005.8:g.158679947G>C	NCBI36
NG_009618.1:g.15113C>G , LRG_71:g.15113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.12C>G	ENSP00000512849.1:p.Ala4=
ENST00000696751.1:c.*137C>G	ENSP00000512850.1:n.*137C>G
ENST00000231228.3:c.642C>G MANE Select	ENSP00000231228.2:p.Ala214=
ENST00000231228.2:c.642C>G	ENSP00000231228.2:p.Ala214=
NM_002187.2:c.642C>G , LRG_71t1:c.642C>G	NP_002178.2:p.Ala214=
NM_002187.3:c.642C>G MANE Select	NP_002178.2:p.Ala214=