Canonical Allele Identifier: CA2676264211

Gene: IL12B

Linked Data

• gnomAD v4: 5-159314956-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159314956C>A , CM000667.2:g.159314956C>A	GRCh38
NC_000005.9:g.158741964C>A , CM000667.1:g.158741964C>A	GRCh37
NC_000005.8:g.158674542C>A	NCBI36
NG_009618.1:g.20518G>T , LRG_71:g.20518G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.*1145G>T	ENSP00000512849.1:n.*1145G>T
ENST00000696751.1:c.*1627G>T	ENSP00000512850.1:n.*1627G>T
ENST00000231228.3:c.*1145G>T MANE Select	ENSP00000231228.2:n.*1145G>T
ENST00000231228.2:c.*1145G>T	ENSP00000231228.2:n.*1145G>T
NM_002187.2:c.*1145G>T , LRG_71t1:c.*1145G>T	NP_002178.2:n.*1145G>T
XR_941138.1:n.364-262C>A
XR_941138.2:n.431-262C>A
NM_002187.3:c.*1145G>T MANE Select	NP_002178.2:n.*1145G>T