Canonical Allele Identifier: CA447681106
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158750327T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323319T>C , CM000667.2:g.159323319T>C GRCh38
NC_000005.9:g.158750327T>C , CM000667.1:g.158750327T>C GRCh37
NC_000005.8:g.158682905T>C NCBI36
NG_009618.1:g.12155A>G , LRG_71:g.12155A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2799A>G ENSP00000512849.1:n.-148-2799A>G
ENST00000696751.1:c.99A>G ENSP00000512850.1:p.Val33=
ENST00000231228.3:c.99A>G MANE Select ENSP00000231228.2:p.Val33=
ENST00000231228.2:c.99A>G ENSP00000231228.2:p.Val33=
NM_002187.2:c.99A>G , LRG_71t1:c.99A>G NP_002178.2:p.Val33=
XR_001742945.1:n.148-2215T>C
NM_002187.3:c.99A>G MANE Select NP_002178.2:p.Val33=