Canonical Allele Identifier: CA2676265370
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323434-T-TG
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323434_159323435insG , CM000667.2:g.159323434_159323435insG GRCh38
NC_000005.9:g.158750442_158750443insG , CM000667.1:g.158750442_158750443insG GRCh37
NC_000005.8:g.158683020_158683021insG NCBI36
NG_009618.1:g.12039_12040insC , LRG_71:g.12039_12040insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2915_-148-2914insC ENSP00000512849.1:n.-148-2915_-148-2914insC
ENST00000696751.1:c.89-106_89-105insC ENSP00000512850.1:n.89-106_89-105insC
ENST00000231228.3:c.89-106_89-105insC MANE Select ENSP00000231228.2:n.89-106_89-105insC
ENST00000231228.2:c.89-106_89-105insC ENSP00000231228.2:n.89-106_89-105insC
NM_002187.2:c.89-106_89-105insC , LRG_71t1:c.89-106_89-105insC NP_002178.2:n.89-106_89-105insC
XR_001742945.1:n.148-2100_148-2099insG
NM_002187.3:c.89-106_89-105insC MANE Select NP_002178.2:n.89-106_89-105insC
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