Canonical Allele Identifier: CA447510897

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747375C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320367C>G , CM000667.2:g.159320367C>G	GRCh38
NC_000005.9:g.158747375C>G , CM000667.1:g.158747375C>G	GRCh37
NC_000005.8:g.158679953C>G	NCBI36
NG_009618.1:g.15107G>C , LRG_71:g.15107G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.6G>C	ENSP00000512849.1:p.Val2=
ENST00000696751.1:c.*131G>C	ENSP00000512850.1:n.*131G>C
ENST00000231228.3:c.636G>C MANE Select	ENSP00000231228.2:p.Val212=
ENST00000231228.2:c.636G>C	ENSP00000231228.2:p.Val212=
NM_002187.2:c.636G>C , LRG_71t1:c.636G>C	NP_002178.2:p.Val212=
NM_002187.3:c.636G>C MANE Select	NP_002178.2:p.Val212=