Canonical Allele Identifier: CA806395048
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1486714185

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327138C>A , CM000667.2:g.159327138C>A GRCh38
NC_000005.9:g.158754146C>A , CM000667.1:g.158754146C>A GRCh37
NC_000005.8:g.158686724C>A NCBI36
NG_009618.1:g.8336G>T , LRG_71:g.8336G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3294G>T ENSP00000512849.1:n.-149+3294G>T
ENST00000696751.1:c.1-356G>T ENSP00000512850.1:n.1-356G>T
ENST00000696752.1:n.433-356G>T
ENST00000231228.3:c.1-356G>T MANE Select ENSP00000231228.2:n.1-356G>T
ENST00000231228.2:c.1-356G>T ENSP00000231228.2:n.1-356G>T
NM_002187.2:c.1-356G>T , LRG_71t1:c.1-356G>T NP_002178.2:n.1-356G>T
NM_002187.3:c.1-356G>T MANE Select NP_002178.2:n.1-356G>T