Canonical Allele Identifier: CA129831607
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1029383857
MyVariant Identifiers: chr5:g.159327317T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327317T>C , CM000667.2:g.159327317T>C GRCh38
NC_000005.9:g.158754325T>C , CM000667.1:g.158754325T>C GRCh37
NC_000005.8:g.158686903T>C NCBI36
NG_009618.1:g.8157A>G , LRG_71:g.8157A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-149+3115A>G ENSP00000512849.1:n.-149+3115A>G
ENST00000696751.1:c.1-535A>G ENSP00000512850.1:n.1-535A>G
ENST00000696752.1:n.433-535A>G
ENST00000231228.3:c.1-535A>G MANE Select ENSP00000231228.2:n.1-535A>G
ENST00000231228.2:c.1-535A>G ENSP00000231228.2:n.1-535A>G
NM_002187.2:c.1-535A>G , LRG_71t1:c.1-535A>G NP_002178.2:n.1-535A>G
NM_002187.3:c.1-535A>G MANE Select NP_002178.2:n.1-535A>G
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