Canonical Allele Identifier: CA2566420319
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159327452_159327453insAACTG , CM000667.2:g.159327452_159327453insAACTG GRCh38
NC_000005.9:g.158754460_158754461insAACTG , CM000667.1:g.158754460_158754461insAACTG GRCh37
NC_000005.8:g.158687038_158687039insAACTG NCBI36
NG_009618.1:g.8021_8022insCAGTT , LRG_71:g.8021_8022insCAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+2979_-149+2980insCAGTT ENSP00000512849.1:n.-149+2979_-149+2980insCAGTT
ENST00000696751.1:c.1-671_1-670insCAGTT ENSP00000512850.1:n.1-671_1-670insCAGTT
ENST00000696752.1:n.433-671_433-670insCAGTT
ENST00000231228.3:c.1-671_1-670insCAGTT MANE Select ENSP00000231228.2:n.1-671_1-670insCAGTT
ENST00000231228.2:c.1-671_1-670insCAGTT ENSP00000231228.2:n.1-671_1-670insCAGTT
NM_002187.2:c.1-671_1-670insCAGTT , LRG_71t1:c.1-671_1-670insCAGTT NP_002178.2:n.1-671_1-670insCAGTT
NM_002187.3:c.1-671_1-670insCAGTT MANE Select NP_002178.2:n.1-671_1-670insCAGTT
Search 100 bp 5'
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