Canonical Allele Identifier: CA3538691
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs11574790

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316838G>A , CM000667.2:g.159316838G>A GRCh38
NC_000005.9:g.158743846G>A , CM000667.1:g.158743846G>A GRCh37
NC_000005.8:g.158676424G>A NCBI36
NG_009618.1:g.18636C>T , LRG_71:g.18636C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000231228.3:c.856-22C>T MANE Select ENSP00000231228.2:p.=
ENST00000231228.2:c.856-22C>T ENSP00000231228.2:p.=
NM_002187.2:c.856-22C>T , LRG_71t1:c.856-22C>T NP_002178.2:p.=
NM_002187.3:c.856-22C>T MANE Select NP_002178.2:p.=