Canonical Allele Identifier: CA1595017366
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320578_159320579delinsAT , CM000667.2:g.159320578_159320579delinsAT GRCh38
NC_000005.9:g.158747586_158747587delinsAT , CM000667.1:g.158747586_158747587delinsAT GRCh37
NC_000005.8:g.158680164_158680165delinsAT NCBI36
NG_009618.1:g.14895_14896delinsAT , LRG_71:g.14895_14896delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-59_-148-58delinsAT ENSP00000512849.1:n.-148-59_-148-58delins...
ENST00000696751.1:c.365-59_365-58delinsAT ENSP00000512850.1:n.365-59_365-58delinsAT...
ENST00000231228.3:c.483-59_483-58delinsAT MANE Select ENSP00000231228.2:n.483-59_483-58delinsAT...
ENST00000231228.2:c.483-59_483-58delinsAT ENSP00000231228.2:n.483-59_483-58delinsAT...
NM_002187.2:c.483-59_483-58delinsAT , LRG_71t1:c.483-59_483-58delinsAT NP_002178.2:n.483-59_483-58delinsAT
XR_001742945.1:n.129_130delinsAT
NM_002187.3:c.483-59_483-58delinsAT MANE Select NP_002178.2:n.483-59_483-58delinsAT