Canonical Allele Identifier: CA362033047

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158747529C>A (hg19) ; chr5:g.159320521C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320521C>A , CM000667.2:g.159320521C>A	GRCh38
NC_000005.9:g.158747529C>A , CM000667.1:g.158747529C>A	GRCh37
NC_000005.8:g.158680107C>A	NCBI36
NG_009618.1:g.14953G>T , LRG_71:g.14953G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-1G>T	ENSP00000512849.1:n.-148-1G>T
ENST00000696751.1:c.365-1G>T	ENSP00000512850.1:n.365-1G>T
ENST00000231228.3:c.483-1G>T MANE Select	ENSP00000231228.2:n.483-1G>T
ENST00000231228.2:c.483-1G>T	ENSP00000231228.2:n.483-1G>T
NM_002187.2:c.483-1G>T , LRG_71t1:c.483-1G>T	NP_002178.2:n.483-1G>T
XR_001742945.1:n.72C>A
NM_002187.3:c.483-1G>T MANE Select	NP_002178.2:n.483-1G>T