Canonical Allele Identifier: CA2676266183

Gene: IL12B

Linked Data

• gnomAD v4: 5-159322660-C-CAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322661_159322662insAAAAAAAAAAAAA , CM000667.2:g.159322661_159322662insAAAAAAAAAAAAA	GRCh38
NC_000005.9:g.158749669_158749670insAAAAAAAAAAAAA , CM000667.1:g.158749669_158749670insAAAAAAAAAAAAA	GRCh37
NC_000005.8:g.158682247_158682248insAAAAAAAAAAAAA	NCBI36
NG_009618.1:g.12813_12814insTTTTTTTTTTTTT , LRG_71:g.12813_12814insTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2141_-148-2140insTTTTTTTTTTTTT	ENSP00000512849.1:n.-148-2141_-148-2140insTTTTTTTTTTTTT
ENST00000696751.1:c.364+393_364+394insTTTTTTTTTTTTT	ENSP00000512850.1:n.364+393_364+394insTTTTTTTTTTTTT
ENST00000231228.3:c.365-150_365-149insTTTTTTTTTTTTT MANE Select	ENSP00000231228.2:n.365-150_365-149insTTTTTTTTTTTTT
ENST00000231228.2:c.365-150_365-149insTTTTTTTTTTTTT	ENSP00000231228.2:n.365-150_365-149insTTTTTTTTTTTTT
NM_002187.2:c.365-150_365-149insTTTTTTTTTTTTT , LRG_71t1:c.365-150_365-149insTTTTTTTTTTTTT	NP_002178.2:n.365-150_365-149insTTTTTTTTTTTTT
XR_001742945.1:n.147+2065_147+2066insAAAAAAAAAAAAA
NM_002187.3:c.365-150_365-149insTTTTTTTTTTTTT MANE Select	NP_002178.2:n.365-150_365-149insTTTTTTTTTTTTT