Canonical Allele Identifier: CA129828874

Gene: IL12B

Linked Data

• dbSNP Id: rs199931878
• gnomAD v4: 5-159323419-TA-T
• MyVariant Identifiers: chr5:g.158750428del (hg19) ; chr5:g.159323420del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323422del , CM000667.2:g.159323422del	GRCh38
NC_000005.9:g.158750430del , CM000667.1:g.158750430del	GRCh37
NC_000005.8:g.158683008del	NCBI36
NG_009618.1:g.12054del , LRG_71:g.12054del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2900del	ENSP00000512849.1:n.-148-2900del
ENST00000696751.1:c.89-91del	ENSP00000512850.1:n.89-91del
ENST00000231228.3:c.89-91del MANE Select	ENSP00000231228.2:n.89-91del
ENST00000231228.2:c.89-91del	ENSP00000231228.2:n.89-91del
NM_002187.2:c.89-91del , LRG_71t1:c.89-91del	NP_002178.2:n.89-91del
XR_001742945.1:n.148-2112del
NM_002187.3:c.89-91del MANE Select	NP_002178.2:n.89-91del