Canonical Allele Identifier: CA806395941

Gene: IL12B

Linked Data

• dbSNP Id: rs1302545392
• MyVariant Identifiers: chr5:g.158755674G>A (hg19) ; chr5:g.159328666G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328666G>A , CM000667.2:g.159328666G>A	GRCh38
NC_000005.9:g.158755674G>A , CM000667.1:g.158755674G>A	GRCh37
NC_000005.8:g.158688252G>A	NCBI36
NG_009618.1:g.6808C>T , LRG_71:g.6808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1766C>T	ENSP00000512849.1:n.-149+1766C>T
ENST00000696751.1:c.-1+1766C>T	ENSP00000512850.1:n.-1+1766C>T
ENST00000696752.1:n.432+1766C>T
ENST00000231228.3:c.-1+1766C>T MANE Select	ENSP00000231228.2:n.-1+1766C>T
ENST00000231228.2:c.-1+1766C>T	ENSP00000231228.2:n.-1+1766C>T
NM_002187.2:c.-1+1766C>T , LRG_71t1:c.-1+1766C>T	NP_002178.2:n.-1+1766C>T
NM_002187.3:c.-1+1766C>T MANE Select	NP_002178.2:n.-1+1766C>T