Canonical Allele Identifier: CA2676265403

Gene: IL12B

Linked Data

• gnomAD v4: 5-159323480-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323480T>C , CM000667.2:g.159323480T>C	GRCh38
NC_000005.9:g.158750488T>C , CM000667.1:g.158750488T>C	GRCh37
NC_000005.8:g.158683066T>C	NCBI36
NG_009618.1:g.11994A>G , LRG_71:g.11994A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2960A>G	ENSP00000512849.1:n.-148-2960A>G
ENST00000696751.1:c.89-151A>G	ENSP00000512850.1:n.89-151A>G
ENST00000231228.3:c.89-151A>G MANE Select	ENSP00000231228.2:n.89-151A>G
ENST00000231228.2:c.89-151A>G	ENSP00000231228.2:n.89-151A>G
NM_002187.2:c.89-151A>G , LRG_71t1:c.89-151A>G	NP_002178.2:n.89-151A>G
XR_001742945.1:n.148-2054T>C
NM_002187.3:c.89-151A>G MANE Select	NP_002178.2:n.89-151A>G