Canonical Allele Identifier: CA1595018456
Gene: IL12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159323036C= , CM000667.2:g.159323036C= GRCh38
NC_000005.9:g.158750044C= , CM000667.1:g.158750044C= GRCh37
NC_000005.8:g.158682622C= NCBI36
NG_009618.1:g.12438G= , LRG_71:g.12438G=

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.-148-2516G= ENSP00000512849.1:n.-148-2516G=
ENST00000696751.1:c.364+18G= ENSP00000512850.1:n.364+18G=
ENST00000231228.3:c.364+18G= MANE Select ENSP00000231228.2:n.364+18G=
ENST00000231228.2:c.364+18G= ENSP00000231228.2:n.364+18G=
NM_002187.2:c.364+18G= , LRG_71t1:c.364+18G= NP_002178.2:n.364+18G=
XR_001742945.1:n.147+2440C=
NM_002187.3:c.364+18G= MANE Select NP_002178.2:n.364+18G=