Canonical Allele Identifier: CA129828881
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs926258216
MyVariant Identifiers: chr5:g.159323431T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323431T>G , CM000667.2:g.159323431T>G GRCh38
NC_000005.9:g.158750439T>G , CM000667.1:g.158750439T>G GRCh37
NC_000005.8:g.158683017T>G NCBI36
NG_009618.1:g.12043A>C , LRG_71:g.12043A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2911A>C ENSP00000512849.1:n.-148-2911A>C
ENST00000696751.1:c.89-102A>C ENSP00000512850.1:n.89-102A>C
ENST00000231228.3:c.89-102A>C MANE Select ENSP00000231228.2:n.89-102A>C
ENST00000231228.2:c.89-102A>C ENSP00000231228.2:n.89-102A>C
NM_002187.2:c.89-102A>C , LRG_71t1:c.89-102A>C NP_002178.2:n.89-102A>C
XR_001742945.1:n.148-2103T>G
NM_002187.3:c.89-102A>C MANE Select NP_002178.2:n.89-102A>C
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