Canonical Allele Identifier: CA362032686

Gene: IL12B

Linked Data

• dbSNP Id: rs763525702
• gnomAD v4: 5-159320405-G-A
• MyVariant Identifiers: chr5:g.158747413G>A (hg19) ; chr5:g.159320405G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159320405G>A , CM000667.2:g.159320405G>A	GRCh38
NC_000005.9:g.158747413G>A , CM000667.1:g.158747413G>A	GRCh37
NC_000005.8:g.158679991G>A	NCBI36
NG_009618.1:g.15069C>T , LRG_71:g.15069C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-33C>T	ENSP00000512849.1:n.-33C>T
ENST00000696751.1:c.*93C>T	ENSP00000512850.1:n.*93C>T
ENST00000231228.3:c.598C>T MANE Select	ENSP00000231228.2:p.Pro200Ser
ENST00000231228.2:c.598C>T	ENSP00000231228.2:p.Pro200Ser
NM_002187.2:c.598C>T , LRG_71t1:c.598C>T	NP_002178.2:p.Pro200Ser
NM_002187.3:c.598C>T MANE Select	NP_002178.2:p.Pro200Ser