Canonical Allele Identifier: CA2676265782
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159326859_159326860insTATT , CM000667.2:g.159326859_159326860insTATT GRCh38
NC_000005.9:g.158753867_158753868insTATT , CM000667.1:g.158753867_158753868insTATT GRCh37
NC_000005.8:g.158686445_158686446insTATT NCBI36
NG_009618.1:g.8615_8616insATAA , LRG_71:g.8615_8616insATAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+3573_-149+3574insATAA ENSP00000512849.1:n.-149+3573_-149+3574insATAA
ENST00000696751.1:c.1-77_1-76insATAA ENSP00000512850.1:n.1-77_1-76insATAA
ENST00000696752.1:n.433-77_433-76insATAA
ENST00000231228.3:c.1-77_1-76insATAA MANE Select ENSP00000231228.2:n.1-77_1-76insATAA
ENST00000231228.2:c.1-77_1-76insATAA ENSP00000231228.2:n.1-77_1-76insATAA
NM_002187.2:c.1-77_1-76insATAA , LRG_71t1:c.1-77_1-76insATAA NP_002178.2:n.1-77_1-76insATAA
NM_002187.3:c.1-77_1-76insATAA MANE Select NP_002178.2:n.1-77_1-76insATAA