Canonical Allele Identifier: CA806396022

Gene: IL12B

Linked Data

• dbSNP Id: rs1301657487
• gnomAD v3: 5-159328802-C-T
• gnomAD v4: 5-159328802-C-T
• MyVariant Identifiers: chr5:g.158755810C>T (hg19) ; chr5:g.159328802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159328802C>T , CM000667.2:g.159328802C>T	GRCh38
NC_000005.9:g.158755810C>T , CM000667.1:g.158755810C>T	GRCh37
NC_000005.8:g.158688388C>T	NCBI36
NG_009618.1:g.6672G>A , LRG_71:g.6672G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-149+1630G>A	ENSP00000512849.1:n.-149+1630G>A
ENST00000696751.1:c.-1+1630G>A	ENSP00000512850.1:n.-1+1630G>A
ENST00000696752.1:n.432+1630G>A
ENST00000231228.3:c.-1+1630G>A MANE Select	ENSP00000231228.2:n.-1+1630G>A
ENST00000231228.2:c.-1+1630G>A	ENSP00000231228.2:n.-1+1630G>A
NM_002187.2:c.-1+1630G>A , LRG_71t1:c.-1+1630G>A	NP_002178.2:n.-1+1630G>A
NM_002187.3:c.-1+1630G>A MANE Select	NP_002178.2:n.-1+1630G>A