Canonical Allele Identifier: CA362036905

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158750304G>C (hg19) ; chr5:g.159323296G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323296G>C , CM000667.2:g.159323296G>C	GRCh38
NC_000005.9:g.158750304G>C , CM000667.1:g.158750304G>C	GRCh37
NC_000005.8:g.158682882G>C	NCBI36
NG_009618.1:g.12178C>G , LRG_71:g.12178C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2776C>G	ENSP00000512849.1:n.-148-2776C>G
ENST00000696751.1:c.122C>G	ENSP00000512850.1:p.Ala41Gly
ENST00000231228.3:c.122C>G MANE Select	ENSP00000231228.2:p.Ala41Gly
ENST00000231228.2:c.122C>G	ENSP00000231228.2:p.Ala41Gly
NM_002187.2:c.122C>G , LRG_71t1:c.122C>G	NP_002178.2:p.Ala41Gly
XR_001742945.1:n.148-2238G>C
NM_002187.3:c.122C>G MANE Select	NP_002178.2:p.Ala41Gly