Canonical Allele Identifier: CA564024500
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1174514752

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322154_159322162del , CM000667.2:g.159322154_159322162del GRCh38
NC_000005.9:g.158749162_158749170del , CM000667.1:g.158749162_158749170del GRCh37
NC_000005.8:g.158681740_158681748del NCBI36
NG_009618.1:g.13314_13322del , LRG_71:g.13314_13322del

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-1640_-148-1632del ENSP00000512849.1:n.-148-1640_-148-1632de...
ENST00000696751.1:c.364+894_364+902del ENSP00000512850.1:n.364+894_364+902del
ENST00000231228.3:c.482+234_482+242del MANE Select ENSP00000231228.2:n.482+234_482+242del
ENST00000231228.2:c.482+234_482+242del ENSP00000231228.2:n.482+234_482+242del
NM_002187.2:c.482+234_482+242del , LRG_71t1:c.482+234_482+242del NP_002178.2:n.482+234_482+242del
XR_001742945.1:n.147+1558_147+1566del
NM_002187.3:c.482+234_482+242del MANE Select NP_002178.2:n.482+234_482+242del