Canonical Allele Identifier: CA2676266174
Gene: IL12B HGNC NCBI

Linked Data

gnomAD v4: 5-159322658-C-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159322658C>G , CM000667.2:g.159322658C>G GRCh38
NC_000005.9:g.158749666C>G , CM000667.1:g.158749666C>G GRCh37
NC_000005.8:g.158682244C>G NCBI36
NG_009618.1:g.12816G>C , LRG_71:g.12816G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696750.1:c.-148-2138G>C ENSP00000512849.1:n.-148-2138G>C
ENST00000696751.1:c.364+396G>C ENSP00000512850.1:n.364+396G>C
ENST00000231228.3:c.365-147G>C MANE Select ENSP00000231228.2:n.365-147G>C
ENST00000231228.2:c.365-147G>C ENSP00000231228.2:n.365-147G>C
NM_002187.2:c.365-147G>C , LRG_71t1:c.365-147G>C NP_002178.2:n.365-147G>C
XR_001742945.1:n.147+2062C>G
NM_002187.3:c.365-147G>C MANE Select NP_002178.2:n.365-147G>C
Search 100 bp 5'
Search 100 bp 3'