Canonical Allele Identifier: CA2769108165
Gene: IL12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322162C>T , CM000667.2:g.159322162C>T GRCh38
NC_000005.9:g.158749170C>T , CM000667.1:g.158749170C>T GRCh37
NC_000005.8:g.158681748C>T NCBI36
NG_009618.1:g.13312G>A , LRG_71:g.13312G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-1642G>A ENSP00000512849.1:n.-148-1642G>A
ENST00000696751.1:c.364+892G>A ENSP00000512850.1:n.364+892G>A
ENST00000231228.3:c.482+232G>A MANE Select ENSP00000231228.2:n.482+232G>A
ENST00000231228.2:c.482+232G>A ENSP00000231228.2:n.482+232G>A
NM_002187.2:c.482+232G>A , LRG_71t1:c.482+232G>A NP_002178.2:n.482+232G>A
XR_001742945.1:n.147+1566C>T
NM_002187.3:c.482+232G>A MANE Select NP_002178.2:n.482+232G>A
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