Canonical Allele Identifier: CA362032979
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159320486-C-T
MyVariant Identifiers: chr5:g.158747494C>T (hg19) chr5:g.159320486C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320486C>T , CM000667.2:g.159320486C>T GRCh38
NC_000005.9:g.158747494C>T , CM000667.1:g.158747494C>T GRCh37
NC_000005.8:g.158680072C>T NCBI36
NG_009618.1:g.14988G>A , LRG_71:g.14988G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-114G>A ENSP00000512849.1:n.-114G>A
ENST00000696751.1:c.*12G>A ENSP00000512850.1:n.*12G>A
ENST00000231228.3:c.517G>A MANE Select ENSP00000231228.2:p.Ala173Thr
ENST00000231228.2:c.517G>A ENSP00000231228.2:p.Ala173Thr
NM_002187.2:c.517G>A , LRG_71t1:c.517G>A NP_002178.2:p.Ala173Thr
XR_001742945.1:n.37C>T
NM_002187.3:c.517G>A MANE Select NP_002178.2:p.Ala173Thr
Search 100 bp 5'
Search 100 bp 3'