Canonical Allele Identifier: CA1083508648

Gene: IL12B

Linked Data

• dbSNP Id: rs1754113081
• gnomAD v3: 5-159322668-T-A
• gnomAD v4: 5-159322668-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322668T>A , CM000667.2:g.159322668T>A	GRCh38
NC_000005.9:g.158749676T>A , CM000667.1:g.158749676T>A	GRCh37
NC_000005.8:g.158682254T>A	NCBI36
NG_009618.1:g.12806A>T , LRG_71:g.12806A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2148A>T	ENSP00000512849.1:n.-148-2148A>T
ENST00000696751.1:c.364+386A>T	ENSP00000512850.1:n.364+386A>T
ENST00000231228.3:c.365-157A>T MANE Select	ENSP00000231228.2:n.365-157A>T
ENST00000231228.2:c.365-157A>T	ENSP00000231228.2:n.365-157A>T
NM_002187.2:c.365-157A>T , LRG_71t1:c.365-157A>T	NP_002178.2:n.365-157A>T
XR_001742945.1:n.147+2072T>A
NM_002187.3:c.365-157A>T MANE Select	NP_002178.2:n.365-157A>T