Canonical Allele Identifier: CA2676264649

Gene: IL12B

Linked Data

• gnomAD v4: 5-159316201-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159316201A>T , CM000667.2:g.159316201A>T	GRCh38
NC_000005.9:g.158743209A>T , CM000667.1:g.158743209A>T	GRCh37
NC_000005.8:g.158675787A>T	NCBI36
NG_009618.1:g.19273T>A , LRG_71:g.19273T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.*1-101T>A	ENSP00000512849.1:n.*1-101T>A
ENST00000696751.1:c.*483-101T>A	ENSP00000512850.1:n.*483-101T>A
ENST00000231228.3:c.*1-101T>A MANE Select	ENSP00000231228.2:n.*1-101T>A
ENST00000231228.2:c.*1-101T>A	ENSP00000231228.2:n.*1-101T>A
NM_002187.2:c.*1-101T>A , LRG_71t1:c.*1-101T>A	NP_002178.2:n.*1-101T>A
NM_002187.3:c.*1-101T>A MANE Select	NP_002178.2:n.*1-101T>A