Canonical Allele Identifier: CA1595045221
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1368439

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315006G>C , CM000667.2:g.159315006G>C GRCh38
NC_000005.9:g.158742014G>C , CM000667.1:g.158742014G>C GRCh37
NC_000005.8:g.158674592G>C NCBI36
NG_009618.1:g.20468C>G , LRG_71:g.20468C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*1095C>G ENSP00000512849.1:n.*1095C>G
ENST00000696751.1:c.*1577C>G ENSP00000512850.1:n.*1577C>G
ENST00000231228.3:c.*1095C>G MANE Select ENSP00000231228.2:n.*1095C>G
ENST00000231228.2:c.*1095C>G ENSP00000231228.2:n.*1095C>G
NM_002187.2:c.*1095C>G , LRG_71t1:c.*1095C>G NP_002178.2:n.*1095C>G
XR_941138.1:n.364-212G>C
XR_941138.2:n.431-212G>C
NM_002187.3:c.*1095C>G MANE Select NP_002178.2:n.*1095C>G