Canonical Allele Identifier: CA2710492038

Gene: IL12B

Linked Data

• dbSNP Id: rs2113029302

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159322633G>A , CM000667.2:g.159322633G>A	GRCh38
NC_000005.9:g.158749641G>A , CM000667.1:g.158749641G>A	GRCh37
NC_000005.8:g.158682219G>A	NCBI36
NG_009618.1:g.12841C>T , LRG_71:g.12841C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2113C>T	ENSP00000512849.1:n.-148-2113C>T
ENST00000696751.1:c.364+421C>T	ENSP00000512850.1:n.364+421C>T
ENST00000231228.3:c.365-122C>T MANE Select	ENSP00000231228.2:n.365-122C>T
ENST00000231228.2:c.365-122C>T	ENSP00000231228.2:n.365-122C>T
NM_002187.2:c.365-122C>T , LRG_71t1:c.365-122C>T	NP_002178.2:n.365-122C>T
XR_001742945.1:n.147+2037G>A
NM_002187.3:c.365-122C>T MANE Select	NP_002178.2:n.365-122C>T