Canonical Allele Identifier: CA129827104

Gene: IL12B

Linked Data

• dbSNP Id: rs905889430
• gnomAD v3: 5-159320653-C-G
• gnomAD v4: 5-159320653-C-G
• MyVariant Identifiers: chr5:g.158747661C>G (hg19) ; chr5:g.159320653C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320653C>G , CM000667.2:g.159320653C>G	GRCh38
NC_000005.9:g.158747661C>G , CM000667.1:g.158747661C>G	GRCh37
NC_000005.8:g.158680239C>G	NCBI36
NG_009618.1:g.14821G>C , LRG_71:g.14821G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-133G>C	ENSP00000512849.1:n.-148-133G>C
ENST00000696751.1:c.365-133G>C	ENSP00000512850.1:n.365-133G>C
ENST00000231228.3:c.483-133G>C MANE Select	ENSP00000231228.2:n.483-133G>C
ENST00000231228.2:c.483-133G>C	ENSP00000231228.2:n.483-133G>C
NM_002187.2:c.483-133G>C , LRG_71t1:c.483-133G>C	NP_002178.2:n.483-133G>C
XR_001742945.1:n.147+57C>G
NM_002187.3:c.483-133G>C MANE Select	NP_002178.2:n.483-133G>C