Canonical Allele Identifier: CA129827815
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs994139883

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159321996C>G , CM000667.2:g.159321996C>G GRCh38
NC_000005.9:g.158749004C>G , CM000667.1:g.158749004C>G GRCh37
NC_000005.8:g.158681582C>G NCBI36
NG_009618.1:g.13478G>C , LRG_71:g.13478G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1476G>C ENSP00000512849.1:n.-148-1476G>C
ENST00000696751.1:c.364+1058G>C ENSP00000512850.1:n.364+1058G>C
ENST00000231228.3:c.482+398G>C MANE Select ENSP00000231228.2:n.482+398G>C
ENST00000231228.2:c.482+398G>C ENSP00000231228.2:n.482+398G>C
NM_002187.2:c.482+398G>C , LRG_71t1:c.482+398G>C NP_002178.2:n.482+398G>C
XR_001742945.1:n.147+1400C>G
NM_002187.3:c.482+398G>C MANE Select NP_002178.2:n.482+398G>C