Canonical Allele Identifier: CA362035265
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158750125G>T (hg19) chr5:g.159323117G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323117G>T , CM000667.2:g.159323117G>T GRCh38
NC_000005.9:g.158750125G>T , CM000667.1:g.158750125G>T GRCh37
NC_000005.8:g.158682703G>T NCBI36
NG_009618.1:g.12357C>A , LRG_71:g.12357C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2597C>A ENSP00000512849.1:n.-148-2597C>A
ENST00000696751.1:c.301C>A ENSP00000512850.1:p.Leu101Ile
ENST00000231228.3:c.301C>A MANE Select ENSP00000231228.2:p.Leu101Ile
ENST00000231228.2:c.301C>A ENSP00000231228.2:p.Leu101Ile
NM_002187.2:c.301C>A , LRG_71t1:c.301C>A NP_002178.2:p.Leu101Ile
XR_001742945.1:n.148-2417G>T
NM_002187.3:c.301C>A MANE Select NP_002178.2:p.Leu101Ile
Search 100 bp 5'
Search 100 bp 3'