Canonical Allele Identifier: CA2676264591
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159316071T>C , CM000667.2:g.159316071T>C GRCh38
NC_000005.9:g.158743079T>C , CM000667.1:g.158743079T>C GRCh37
NC_000005.8:g.158675657T>C NCBI36
NG_009618.1:g.19403A>G , LRG_71:g.19403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.*30A>G ENSP00000512849.1:n.*30A>G
ENST00000696751.1:c.*512A>G ENSP00000512850.1:n.*512A>G
ENST00000231228.3:c.*30A>G MANE Select ENSP00000231228.2:n.*30A>G
ENST00000231228.2:c.*30A>G ENSP00000231228.2:n.*30A>G
NM_002187.2:c.*30A>G , LRG_71t1:c.*30A>G NP_002178.2:n.*30A>G
NM_002187.3:c.*30A>G MANE Select NP_002178.2:n.*30A>G