Canonical Allele Identifier: CA1083508635
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs1754112290
gnomAD v3: 5-159322634-T-TA
gnomAD v4: 5-159322634-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322635dup , CM000667.2:g.159322635dup GRCh38
NC_000005.9:g.158749643dup , CM000667.1:g.158749643dup GRCh37
NC_000005.8:g.158682221dup NCBI36
NG_009618.1:g.12839dup , LRG_71:g.12839dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2115dup ENSP00000512849.1:n.-148-2115dup
ENST00000696751.1:c.364+419dup ENSP00000512850.1:n.364+419dup
ENST00000231228.3:c.365-124dup MANE Select ENSP00000231228.2:n.365-124dup
ENST00000231228.2:c.365-124dup ENSP00000231228.2:n.365-124dup
NM_002187.2:c.365-124dup , LRG_71t1:c.365-124dup NP_002178.2:n.365-124dup
XR_001742945.1:n.147+2039dup
NM_002187.3:c.365-124dup MANE Select NP_002178.2:n.365-124dup
Search 100 bp 5'
Search 100 bp 3'