Canonical Allele Identifier: CA1595045690
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315981_159315990delinsAAAAAACGTT , CM000667.2:g.159315981_159315990delinsAAAAAACGTT GRCh38
NC_000005.9:g.158742989_158742998delinsAAAAAACGTT , CM000667.1:g.158742989_158742998delinsAAAAAACGTT GRCh37
NC_000005.8:g.158675567_158675576delinsAAAAAACGTT NCBI36
NG_009618.1:g.19484_19493delinsAACGTTTTTT , LRG_71:g.19484_19493delinsAACGTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*111_*120delinsAACGTTTTTT ENSP00000512849.1:n.*111_*120delinsAACGTT...
ENST00000696751.1:c.*593_*602delinsAACGTTTTTT ENSP00000512850.1:n.*593_*602delinsAACGTT...
ENST00000231228.3:c.*111_*120delinsAACGTTTTTT MANE Select ENSP00000231228.2:n.*111_*120delinsAACGTT...
ENST00000231228.2:c.*111_*120delinsAACGTTTTTT ENSP00000231228.2:n.*111_*120delinsAACGTT...
NM_002187.2:c.*111_*120delinsAACGTTTTTT , LRG_71t1:c.*111_*120delinsAACGTTTTTT NP_002178.2:n.*111_*120delinsAACGTTTTTT
NM_002187.3:c.*111_*120delinsAACGTTTTTT MANE Select NP_002178.2:n.*111_*120delinsAACGTTTTTT