Canonical Allele Identifier: CA1595020176
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327212_159327213delinsGA , CM000667.2:g.159327212_159327213delinsGA GRCh38
NC_000005.9:g.158754220_158754221delinsGA , CM000667.1:g.158754220_158754221delinsGA GRCh37
NC_000005.8:g.158686798_158686799delinsGA NCBI36
NG_009618.1:g.8261_8262delinsTC , LRG_71:g.8261_8262delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3219_-149+3220delinsTC ENSP00000512849.1:n.-149+3219_-149+3220de...
ENST00000696751.1:c.1-431_1-430delinsTC ENSP00000512850.1:n.1-431_1-430delinsTC
ENST00000696752.1:n.433-431_433-430delinsTC
ENST00000231228.3:c.1-431_1-430delinsTC MANE Select ENSP00000231228.2:n.1-431_1-430delinsTC
ENST00000231228.2:c.1-431_1-430delinsTC ENSP00000231228.2:n.1-431_1-430delinsTC
NM_002187.2:c.1-431_1-430delinsTC , LRG_71t1:c.1-431_1-430delinsTC NP_002178.2:n.1-431_1-430delinsTC
NM_002187.3:c.1-431_1-430delinsTC MANE Select NP_002178.2:n.1-431_1-430delinsTC