Canonical Allele Identifier: CA362035758

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158750172G>A (hg19) ; chr5:g.159323164G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323164G>A , CM000667.2:g.159323164G>A	GRCh38
NC_000005.9:g.158750172G>A , CM000667.1:g.158750172G>A	GRCh37
NC_000005.8:g.158682750G>A	NCBI36
NG_009618.1:g.12310C>T , LRG_71:g.12310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2644C>T	ENSP00000512849.1:n.-148-2644C>T
ENST00000696751.1:c.254C>T	ENSP00000512850.1:p.Ala85Val
ENST00000231228.3:c.254C>T MANE Select	ENSP00000231228.2:p.Ala85Val
ENST00000231228.2:c.254C>T	ENSP00000231228.2:p.Ala85Val
NM_002187.2:c.254C>T , LRG_71t1:c.254C>T	NP_002178.2:p.Ala85Val
XR_001742945.1:n.148-2370G>A
NM_002187.3:c.254C>T MANE Select	NP_002178.2:p.Ala85Val