Canonical Allele Identifier: CA447681112
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158750333A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323325A>G , CM000667.2:g.159323325A>G GRCh38
NC_000005.9:g.158750333A>G , CM000667.1:g.158750333A>G GRCh37
NC_000005.8:g.158682911A>G NCBI36
NG_009618.1:g.12149T>C , LRG_71:g.12149T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2805T>C ENSP00000512849.1:n.-148-2805T>C
ENST00000696751.1:c.93T>C ENSP00000512850.1:p.Tyr31=
ENST00000231228.3:c.93T>C MANE Select ENSP00000231228.2:p.Tyr31=
ENST00000231228.2:c.93T>C ENSP00000231228.2:p.Tyr31=
NM_002187.2:c.93T>C , LRG_71t1:c.93T>C NP_002178.2:p.Tyr31=
XR_001742945.1:n.148-2209A>G
NM_002187.3:c.93T>C MANE Select NP_002178.2:p.Tyr31=