Canonical Allele Identifier: CA362036914

Gene: IL12B

Linked Data

• MyVariant Identifiers: chr5:g.158750305C>G (hg19) ; chr5:g.159323297C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159323297C>G , CM000667.2:g.159323297C>G	GRCh38
NC_000005.9:g.158750305C>G , CM000667.1:g.158750305C>G	GRCh37
NC_000005.8:g.158682883C>G	NCBI36
NG_009618.1:g.12177G>C , LRG_71:g.12177G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-2777G>C	ENSP00000512849.1:n.-148-2777G>C
ENST00000696751.1:c.121G>C	ENSP00000512850.1:p.Ala41Pro
ENST00000231228.3:c.121G>C MANE Select	ENSP00000231228.2:p.Ala41Pro
ENST00000231228.2:c.121G>C	ENSP00000231228.2:p.Ala41Pro
NM_002187.2:c.121G>C , LRG_71t1:c.121G>C	NP_002178.2:p.Ala41Pro
XR_001742945.1:n.148-2237C>G
NM_002187.3:c.121G>C MANE Select	NP_002178.2:p.Ala41Pro