Canonical Allele Identifier: CA806395239
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1367374975
MyVariant Identifiers: chr5:g.158754484C>T (hg19) chr5:g.159327476C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327476C>T , CM000667.2:g.159327476C>T GRCh38
NC_000005.9:g.158754484C>T , CM000667.1:g.158754484C>T GRCh37
NC_000005.8:g.158687062C>T NCBI36
NG_009618.1:g.7998G>A , LRG_71:g.7998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+2956G>A ENSP00000512849.1:n.-149+2956G>A
ENST00000696751.1:c.1-694G>A ENSP00000512850.1:n.1-694G>A
ENST00000696752.1:n.433-694G>A
ENST00000231228.3:c.1-694G>A MANE Select ENSP00000231228.2:n.1-694G>A
ENST00000231228.2:c.1-694G>A ENSP00000231228.2:n.1-694G>A
NM_002187.2:c.1-694G>A , LRG_71t1:c.1-694G>A NP_002178.2:n.1-694G>A
NM_002187.3:c.1-694G>A MANE Select NP_002178.2:n.1-694G>A
Search 100 bp 5'
Search 100 bp 3'