Canonical Allele Identifier: CA1595020779
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs955687219
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159328672C>G , CM000667.2:g.159328672C>G GRCh38
NC_000005.9:g.158755680C>G , CM000667.1:g.158755680C>G GRCh37
NC_000005.8:g.158688258C>G NCBI36
NG_009618.1:g.6802G>C , LRG_71:g.6802G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-149+1760G>C ENSP00000512849.1:n.-149+1760G>C
ENST00000696751.1:c.-1+1760G>C ENSP00000512850.1:n.-1+1760G>C
ENST00000696752.1:n.432+1760G>C
ENST00000231228.3:c.-1+1760G>C MANE Select ENSP00000231228.2:n.-1+1760G>C
ENST00000231228.2:c.-1+1760G>C ENSP00000231228.2:n.-1+1760G>C
NM_002187.2:c.-1+1760G>C , LRG_71t1:c.-1+1760G>C NP_002178.2:n.-1+1760G>C
NM_002187.3:c.-1+1760G>C MANE Select NP_002178.2:n.-1+1760G>C
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