Canonical Allele Identifier: CA129832504
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs993120120

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328863A>G , CM000667.2:g.159328863A>G GRCh38
NC_000005.9:g.158755871A>G , CM000667.1:g.158755871A>G GRCh37
NC_000005.8:g.158688449A>G NCBI36
NG_009618.1:g.6611T>C , LRG_71:g.6611T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+1569T>C ENSP00000512849.1:n.-149+1569T>C
ENST00000696751.1:c.-1+1569T>C ENSP00000512850.1:n.-1+1569T>C
ENST00000696752.1:n.432+1569T>C
ENST00000231228.3:c.-1+1569T>C MANE Select ENSP00000231228.2:n.-1+1569T>C
ENST00000231228.2:c.-1+1569T>C ENSP00000231228.2:n.-1+1569T>C
NM_002187.2:c.-1+1569T>C , LRG_71t1:c.-1+1569T>C NP_002178.2:n.-1+1569T>C
NM_002187.3:c.-1+1569T>C MANE Select NP_002178.2:n.-1+1569T>C