Canonical Allele Identifier: CA362036082
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1562113610

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323195G>C , CM000667.2:g.159323195G>C GRCh38
NC_000005.9:g.158750203G>C , CM000667.1:g.158750203G>C GRCh37
NC_000005.8:g.158682781G>C NCBI36
NG_009618.1:g.12279C>G , LRG_71:g.12279C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2675C>G ENSP00000512849.1:n.-148-2675C>G
ENST00000696751.1:c.223C>G ENSP00000512850.1:p.Leu75Val
ENST00000231228.3:c.223C>G MANE Select ENSP00000231228.2:p.Leu75Val
ENST00000231228.2:c.223C>G ENSP00000231228.2:p.Leu75Val
NM_002187.2:c.223C>G , LRG_71t1:c.223C>G NP_002178.2:p.Leu75Val
XR_001742945.1:n.148-2339G>C
NM_002187.3:c.223C>G MANE Select NP_002178.2:p.Leu75Val