Canonical Allele Identifier: CA12014477
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs3212219
gnomAD v2: 5-158754461-C-A
gnomAD v3: 5-159327453-C-A
gnomAD v4: 5-159327453-C-A
MyVariant Identifiers: chr5:g.158754461C>A (hg19) chr5:g.159327453C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327453C>A , CM000667.2:g.159327453C>A GRCh38
NC_000005.9:g.158754461C>A , CM000667.1:g.158754461C>A GRCh37
NC_000005.8:g.158687039C>A NCBI36
NG_009618.1:g.8021G>T , LRG_71:g.8021G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+2979G>T ENSP00000512849.1:n.-149+2979G>T
ENST00000696751.1:c.1-671G>T ENSP00000512850.1:n.1-671G>T
ENST00000696752.1:n.433-671G>T
ENST00000231228.3:c.1-671G>T MANE Select ENSP00000231228.2:n.1-671G>T
ENST00000231228.2:c.1-671G>T ENSP00000231228.2:n.1-671G>T
NM_002187.2:c.1-671G>T , LRG_71t1:c.1-671G>T NP_002178.2:n.1-671G>T
NM_002187.3:c.1-671G>T MANE Select NP_002178.2:n.1-671G>T
Search 100 bp 5'
Search 100 bp 3'