Canonical Allele Identifier: CA1595020173
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327205_159327207delinsTGA , CM000667.2:g.159327205_159327207delinsTGA GRCh38
NC_000005.9:g.158754213_158754215delinsTGA , CM000667.1:g.158754213_158754215delinsTGA GRCh37
NC_000005.8:g.158686791_158686793delinsTGA NCBI36
NG_009618.1:g.8267_8269delinsTCA , LRG_71:g.8267_8269delinsTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3225_-149+3227delinsTCA ENSP00000512849.1:n.-149+3225_-149+3227de...
ENST00000696751.1:c.1-425_1-423delinsTCA ENSP00000512850.1:n.1-425_1-423delinsTCA
ENST00000696752.1:n.433-425_433-423delinsTCA
ENST00000231228.3:c.1-425_1-423delinsTCA MANE Select ENSP00000231228.2:n.1-425_1-423delinsTCA
ENST00000231228.2:c.1-425_1-423delinsTCA ENSP00000231228.2:n.1-425_1-423delinsTCA
NM_002187.2:c.1-425_1-423delinsTCA , LRG_71t1:c.1-425_1-423delinsTCA NP_002178.2:n.1-425_1-423delinsTCA
NM_002187.3:c.1-425_1-423delinsTCA MANE Select NP_002178.2:n.1-425_1-423delinsTCA