Canonical Allele Identifier: CA2676265664

Gene: IL12B

Linked Data

• gnomAD v4: 5-159322251-A-ATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322251_159322252insTTT , CM000667.2:g.159322251_159322252insTTT	GRCh38
NC_000005.9:g.158749259_158749260insTTT , CM000667.1:g.158749259_158749260insTTT	GRCh37
NC_000005.8:g.158681837_158681838insTTT	NCBI36
NG_009618.1:g.13222_13223insAAA , LRG_71:g.13222_13223insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1732_-148-1731insAAA	ENSP00000512849.1:n.-148-1732_-148-1731insAAA
ENST00000696751.1:c.364+802_364+803insAAA	ENSP00000512850.1:n.364+802_364+803insAAA
ENST00000231228.3:c.482+142_482+143insAAA MANE Select	ENSP00000231228.2:n.482+142_482+143insAAA
ENST00000231228.2:c.482+142_482+143insAAA	ENSP00000231228.2:n.482+142_482+143insAAA
NM_002187.2:c.482+142_482+143insAAA , LRG_71t1:c.482+142_482+143insAAA	NP_002178.2:n.482+142_482+143insAAA
XR_001742945.1:n.147+1655_147+1656insTTT
NM_002187.3:c.482+142_482+143insAAA MANE Select	NP_002178.2:n.482+142_482+143insAAA