Canonical Allele Identifier: CA2676265366
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159323429-C-CTTGT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323432_159323435dup , CM000667.2:g.159323432_159323435dup GRCh38
NC_000005.9:g.158750440_158750443dup , CM000667.1:g.158750440_158750443dup GRCh37
NC_000005.8:g.158683018_158683021dup NCBI36
NG_009618.1:g.12041_12044dup , LRG_71:g.12041_12044dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2913_-148-2910dup ENSP00000512849.1:n.-148-2913_-148-2910dup
ENST00000696751.1:c.89-104_89-101dup ENSP00000512850.1:n.89-104_89-101dup
ENST00000231228.3:c.89-104_89-101dup MANE Select ENSP00000231228.2:n.89-104_89-101dup
ENST00000231228.2:c.89-104_89-101dup ENSP00000231228.2:n.89-104_89-101dup
NM_002187.2:c.89-104_89-101dup , LRG_71t1:c.89-104_89-101dup NP_002178.2:n.89-104_89-101dup
XR_001742945.1:n.148-2102_148-2099dup
NM_002187.3:c.89-104_89-101dup MANE Select NP_002178.2:n.89-104_89-101dup
Search 100 bp 5'
Search 100 bp 3'