Canonical Allele Identifier: CA2676266231

Gene: IL12B

Linked Data

• gnomAD v4: 5-159322939-TTGATGTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322940_159322947del , CM000667.2:g.159322940_159322947del	GRCh38
NC_000005.9:g.158749948_158749955del , CM000667.1:g.158749948_158749955del	GRCh37
NC_000005.8:g.158682526_158682533del	NCBI36
NG_009618.1:g.12527_12534del , LRG_71:g.12527_12534del

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-148-2427_-148-2420del	ENSP00000512849.1:n.-148-2427_-148-2420de...
ENST00000696751.1:c.364+107_364+114del	ENSP00000512850.1:n.364+107_364+114del
ENST00000231228.3:c.364+107_364+114del MANE Select	ENSP00000231228.2:n.364+107_364+114del
ENST00000231228.2:c.364+107_364+114del	ENSP00000231228.2:n.364+107_364+114del
NM_002187.2:c.364+107_364+114del , LRG_71t1:c.364+107_364+114del	NP_002178.2:n.364+107_364+114del
XR_001742945.1:n.147+2344_147+2351del
NM_002187.3:c.364+107_364+114del MANE Select	NP_002178.2:n.364+107_364+114del