Canonical Allele Identifier: CA87008483
Gene: IL12A HGNC NCBI
IL12A-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.159995680G>A
GRCh37 chr3:g.159713467G>A
gnomAD v2:
3:159713467 G / A
gnomAD v3:
3:159995680 G / A
gnomAD v4:
chr3-159995680-G-A
Joint Max Group AF 0.3151459 (SAS)
Genomes Max Group AF 0.31075223 (SAS)
Exomes Max Group AF 0.3139238 (SAS)
dbSNP:
568408
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.159995680G>A , CM000665.2:g.159995680G>A GRCh38
NC_000003.11:g.159713467G>A , CM000665.1:g.159713467G>A GRCh37
NC_000003.10:g.161196161G>A NCBI36
NG_033022.1:g.11845G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699704.1:c.*121G>A (IL12A) MANE Select ENSP00000514529.1:n.*121G>A
ENST00000305579.7:c.*121G>A (IL12A) ENSP00000303231.2:n.*121G>A
ENST00000305579.6:c.*121G>A (IL12A) ENSP00000303231.2:n.*121G>A
ENST00000466512.1:c.*121G>A (IL12A) ENSP00000419046.1:n.*121G>A
ENST00000468862.5:n.1570G>A (IL12A)
NM_000882.3:c.*121G>A (IL12A) NP_000873.2:n.*121G>A
NR_108088.1:n.1085-1375C>T (IL12A-AS1)
NM_001354582.1:c.*121G>A (IL12A) NP_001341511.1:n.*121G>A
NM_001354583.1:c.*121G>A (IL12A) NP_001341512.1:n.*121G>A
NM_000882.4:c.*121G>A (IL12A) NP_000873.2:n.*121G>A
NM_001354582.2:c.*121G>A (IL12A) NP_001341511.1:n.*121G>A
NM_001354583.2:c.*121G>A (IL12A) NP_001341512.1:n.*121G>A
NM_001397992.1:c.*121G>A (IL12A) MANE Select NP_001384921.1:n.*121G>A
Search 100 bp 5'
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