Canonical Allele Identifier: CA447681338
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1357044342

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323292A>C , CM000667.2:g.159323292A>C GRCh38
NC_000005.9:g.158750300A>C , CM000667.1:g.158750300A>C GRCh37
NC_000005.8:g.158682878A>C NCBI36
NG_009618.1:g.12182T>G , LRG_71:g.12182T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2772T>G ENSP00000512849.1:n.-148-2772T>G
ENST00000696751.1:c.126T>G ENSP00000512850.1:p.Pro42=
ENST00000231228.3:c.126T>G MANE Select ENSP00000231228.2:p.Pro42=
ENST00000231228.2:c.126T>G ENSP00000231228.2:p.Pro42=
NM_002187.2:c.126T>G , LRG_71t1:c.126T>G NP_002178.2:p.Pro42=
XR_001742945.1:n.148-2242A>C
NM_002187.3:c.126T>G MANE Select NP_002178.2:p.Pro42=