Canonical Allele Identifier: CA362034761
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158750072C>G (hg19) chr5:g.159323064C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323064C>G , CM000667.2:g.159323064C>G GRCh38
NC_000005.9:g.158750072C>G , CM000667.1:g.158750072C>G GRCh37
NC_000005.8:g.158682650C>G NCBI36
NG_009618.1:g.12410G>C , LRG_71:g.12410G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2544G>C ENSP00000512849.1:n.-148-2544G>C
ENST00000696751.1:c.354G>C ENSP00000512850.1:p.Lys118Asn
ENST00000231228.3:c.354G>C MANE Select ENSP00000231228.2:p.Lys118Asn
ENST00000231228.2:c.354G>C ENSP00000231228.2:p.Lys118Asn
NM_002187.2:c.354G>C , LRG_71t1:c.354G>C NP_002178.2:p.Lys118Asn
XR_001742945.1:n.147+2468C>G
NM_002187.3:c.354G>C MANE Select NP_002178.2:p.Lys118Asn
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