Canonical Allele Identifier: CA362032723
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747421C>T (hg19) chr5:g.159320413C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320413C>T , CM000667.2:g.159320413C>T GRCh38
NC_000005.9:g.158747421C>T , CM000667.1:g.158747421C>T GRCh37
NC_000005.8:g.158679999C>T NCBI36
NG_009618.1:g.15061G>A , LRG_71:g.15061G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-41G>A ENSP00000512849.1:n.-41G>A
ENST00000696751.1:c.*85G>A ENSP00000512850.1:n.*85G>A
ENST00000231228.3:c.590G>A MANE Select ENSP00000231228.2:p.Ser197Asn
ENST00000231228.2:c.590G>A ENSP00000231228.2:p.Ser197Asn
NM_002187.2:c.590G>A , LRG_71t1:c.590G>A NP_002178.2:p.Ser197Asn
NM_002187.3:c.590G>A MANE Select NP_002178.2:p.Ser197Asn
Search 100 bp 5'
Search 100 bp 3'