Canonical Allele Identifier: CA362037063
Gene: IL12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323321C>G , CM000667.2:g.159323321C>G GRCh38
NC_000005.9:g.158750329C>G , CM000667.1:g.158750329C>G GRCh37
NC_000005.8:g.158682907C>G NCBI36
NG_009618.1:g.12153G>C , LRG_71:g.12153G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2801G>C ENSP00000512849.1:n.-148-2801G>C
ENST00000696751.1:c.97G>C ENSP00000512850.1:p.Val33Leu
ENST00000231228.3:c.97G>C MANE Select ENSP00000231228.2:p.Val33Leu
ENST00000231228.2:c.97G>C ENSP00000231228.2:p.Val33Leu
NM_002187.2:c.97G>C , LRG_71t1:c.97G>C NP_002178.2:p.Val33Leu
XR_001742945.1:n.148-2213C>G
NM_002187.3:c.97G>C MANE Select NP_002178.2:p.Val33Leu