Canonical Allele Identifier: CA129823281
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs998639800

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316038G>A , CM000667.2:g.159316038G>A GRCh38
NC_000005.9:g.158743046G>A , CM000667.1:g.158743046G>A GRCh37
NC_000005.8:g.158675624G>A NCBI36
NG_009618.1:g.19436C>T , LRG_71:g.19436C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*63C>T ENSP00000512849.1:n.*63C>T
ENST00000696751.1:c.*545C>T ENSP00000512850.1:n.*545C>T
ENST00000231228.3:c.*63C>T MANE Select ENSP00000231228.2:n.*63C>T
ENST00000231228.2:c.*63C>T ENSP00000231228.2:n.*63C>T
NM_002187.2:c.*63C>T , LRG_71t1:c.*63C>T NP_002178.2:n.*63C>T
NM_002187.3:c.*63C>T MANE Select NP_002178.2:n.*63C>T