Canonical Allele Identifier: CA806395296
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1221168363
MyVariant Identifiers: chr5:g.158754560A>G (hg19) chr5:g.159327552A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327552A>G , CM000667.2:g.159327552A>G GRCh38
NC_000005.9:g.158754560A>G , CM000667.1:g.158754560A>G GRCh37
NC_000005.8:g.158687138A>G NCBI36
NG_009618.1:g.7922T>C , LRG_71:g.7922T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+2880T>C ENSP00000512849.1:n.-149+2880T>C
ENST00000696751.1:c.1-770T>C ENSP00000512850.1:n.1-770T>C
ENST00000696752.1:n.433-770T>C
ENST00000231228.3:c.1-770T>C MANE Select ENSP00000231228.2:n.1-770T>C
ENST00000231228.2:c.1-770T>C ENSP00000231228.2:n.1-770T>C
NM_002187.2:c.1-770T>C , LRG_71t1:c.1-770T>C NP_002178.2:n.1-770T>C
NM_002187.3:c.1-770T>C MANE Select NP_002178.2:n.1-770T>C
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