Canonical Allele Identifier: CA1083508464
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs2853694

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322080G>C , CM000667.2:g.159322080G>C GRCh38
NC_000005.9:g.158749088G>C , CM000667.1:g.158749088G>C GRCh37
NC_000005.8:g.158681666G>C NCBI36
NG_009618.1:g.13394C>G , LRG_71:g.13394C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1560C>G ENSP00000512849.1:n.-148-1560C>G
ENST00000696751.1:c.364+974C>G ENSP00000512850.1:n.364+974C>G
ENST00000231228.3:c.482+314C>G MANE Select ENSP00000231228.2:n.482+314C>G
ENST00000231228.2:c.482+314C>G ENSP00000231228.2:n.482+314C>G
NM_002187.2:c.482+314C>G , LRG_71t1:c.482+314C>G NP_002178.2:n.482+314C>G
XR_001742945.1:n.147+1484G>C
NM_002187.3:c.482+314C>G MANE Select NP_002178.2:n.482+314C>G