Canonical Allele Identifier: CA362032162
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158747313C>G (hg19) chr5:g.159320305C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159320305C>G , CM000667.2:g.159320305C>G GRCh38
NC_000005.9:g.158747313C>G , CM000667.1:g.158747313C>G GRCh37
NC_000005.8:g.158679891C>G NCBI36
NG_009618.1:g.15169G>C , LRG_71:g.15169G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.67+1G>C ENSP00000512849.1:n.67+1G>C
ENST00000696751.1:c.*192+1G>C ENSP00000512850.1:n.*192+1G>C
ENST00000231228.3:c.697+1G>C MANE Select ENSP00000231228.2:n.697+1G>C
ENST00000231228.2:c.697+1G>C ENSP00000231228.2:n.697+1G>C
NM_002187.2:c.697+1G>C , LRG_71t1:c.697+1G>C NP_002178.2:n.697+1G>C
NM_002187.3:c.697+1G>C MANE Select NP_002178.2:n.697+1G>C
Search 100 bp 5'
Search 100 bp 3'