Canonical Allele Identifier: CA447681158
Gene: IL12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.158750123G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323115G>C , CM000667.2:g.159323115G>C GRCh38
NC_000005.9:g.158750123G>C , CM000667.1:g.158750123G>C GRCh37
NC_000005.8:g.158682701G>C NCBI36
NG_009618.1:g.12359C>G , LRG_71:g.12359C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2595C>G ENSP00000512849.1:n.-148-2595C>G
ENST00000696751.1:c.303C>G ENSP00000512850.1:p.Leu101=
ENST00000231228.3:c.303C>G MANE Select ENSP00000231228.2:p.Leu101=
ENST00000231228.2:c.303C>G ENSP00000231228.2:p.Leu101=
NM_002187.2:c.303C>G , LRG_71t1:c.303C>G NP_002178.2:p.Leu101=
XR_001742945.1:n.148-2419G>C
NM_002187.3:c.303C>G MANE Select NP_002178.2:p.Leu101=