Canonical Allele Identifier: CA2520913750

Gene: IL12B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159321982C>A , CM000667.2:g.159321982C>A	GRCh38
NC_000005.9:g.158748990C>A , CM000667.1:g.158748990C>A	GRCh37
NC_000005.8:g.158681568C>A	NCBI36
NG_009618.1:g.13492G>T , LRG_71:g.13492G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696750.1:c.-148-1462G>T	ENSP00000512849.1:n.-148-1462G>T
ENST00000696751.1:c.364+1072G>T	ENSP00000512850.1:n.364+1072G>T
ENST00000231228.3:c.482+412G>T MANE Select	ENSP00000231228.2:n.482+412G>T
ENST00000231228.2:c.482+412G>T	ENSP00000231228.2:n.482+412G>T
NM_002187.2:c.482+412G>T , LRG_71t1:c.482+412G>T	NP_002178.2:n.482+412G>T
XR_001742945.1:n.147+1386C>A
NM_002187.3:c.482+412G>T MANE Select	NP_002178.2:n.482+412G>T