Canonical Allele Identifier: CA806395181
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1463117358
gnomAD v3: 5-159327385-GGGT-G
gnomAD v4: 5-159327385-GGGT-G
MyVariant Identifiers: chr5:g.158754394_158754396del (hg19) chr5:g.159327386_159327388del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327386_159327388del , CM000667.2:g.159327386_159327388del GRCh38
NC_000005.9:g.158754394_158754396del , CM000667.1:g.158754394_158754396del GRCh37
NC_000005.8:g.158686972_158686974del NCBI36
NG_009618.1:g.8086_8088del , LRG_71:g.8086_8088del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+3044_-149+3046del ENSP00000512849.1:n.-149+3044_-149+3046del
ENST00000696751.1:c.1-606_1-604del ENSP00000512850.1:n.1-606_1-604del
ENST00000696752.1:n.433-606_433-604del
ENST00000231228.3:c.1-606_1-604del MANE Select ENSP00000231228.2:n.1-606_1-604del
ENST00000231228.2:c.1-606_1-604del ENSP00000231228.2:n.1-606_1-604del
NM_002187.2:c.1-606_1-604del , LRG_71t1:c.1-606_1-604del NP_002178.2:n.1-606_1-604del
NM_002187.3:c.1-606_1-604del MANE Select NP_002178.2:n.1-606_1-604del
Search 100 bp 5'
Search 100 bp 3'