Canonical Allele Identifier: CA2605806582
Gene: IL12B HGNC NCBI

Linked Data

dbSNP Id: rs2113022179
gnomAD v3: 5-159315908-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159315908A>T , CM000667.2:g.159315908A>T GRCh38
NC_000005.9:g.158742916A>T , CM000667.1:g.158742916A>T GRCh37
NC_000005.8:g.158675494A>T NCBI36
NG_009618.1:g.19566T>A , LRG_71:g.19566T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696750.1:c.*193T>A ENSP00000512849.1:n.*193T>A
ENST00000696751.1:c.*675T>A ENSP00000512850.1:n.*675T>A
ENST00000231228.3:c.*193T>A MANE Select ENSP00000231228.2:n.*193T>A
ENST00000231228.2:c.*193T>A ENSP00000231228.2:n.*193T>A
NM_002187.2:c.*193T>A , LRG_71t1:c.*193T>A NP_002178.2:n.*193T>A
NM_002187.3:c.*193T>A MANE Select NP_002178.2:n.*193T>A
Search 100 bp 5'
Search 100 bp 3'