Canonical Allele Identifier: CA10611444

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 331655
• ClinVar RCV Id: RCV000295649
• dbSNP Id: rs12803
• gnomAD v2: 2-157181925-A-C
• gnomAD v3: 2-156325413-A-C
• gnomAD v4: 2-156325413-A-C
• MyVariant Identifiers: chr2:g.157181925A>C (hg19) ; chr2:g.156325413A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156325413A>C , CM000664.2:g.156325413A>C	GRCh38
NC_000002.11:g.157181925A>C , CM000664.1:g.157181925A>C	GRCh37
NC_000002.10:g.156890171A>C	NCBI36
NG_011821.1:g.12363T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.*331T>G	ENSP00000514865.1:n.*331T>G
ENST00000700229.1:c.1092T>G
ENST00000700230.1:c.1668T>G	ENSP00000514867.1:n.1668T>G
ENST00000700231.1:c.*331T>G	ENSP00000514868.1:n.*331T>G
ENST00000339562.9:c.*331T>G MANE Select	ENSP00000344479.4:n.*331T>G
ENST00000675870.1:c.*639T>G	ENSP00000502739.1:n.*639T>G
ENST00000339562.8:c.*331T>G	ENSP00000344479.4:n.*331T>G
ENST00000409572.5:c.*331T>G	ENSP00000386747.1:n.*331T>G
ENST00000417764.5:c.*639T>G	ENSP00000415632.1:n.*639T>G
ENST00000417972.5:c.*639T>G	ENSP00000394671.1:n.*639T>G
ENST00000426264.5:c.*331T>G	ENSP00000389986.1:n.*331T>G
NM_006186.3:c.*331T>G	NP_006177.1:n.*331T>G
XM_005246621.2:c.*331T>G	XP_005246678.1:n.*331T>G
XM_005246622.2:c.*331T>G	XP_005246679.1:n.*331T>G
XM_005246623.1:c.*331T>G	XP_005246680.1:n.*331T>G
XM_006712553.2:c.*331T>G	XP_006712616.1:n.*331T>G
XM_011511246.1:c.*362T>G	XP_011509548.1:n.*362T>G
NM_173173.2:c.*331T>G	NP_775265.1:n.*331T>G
XM_005246621.4:c.*331T>G	XP_005246678.1:n.*331T>G
XM_006712553.4:c.*331T>G	XP_006712616.1:n.*331T>G
XM_011511246.2:c.*362T>G	XP_011509548.1:n.*362T>G
XM_017004219.2:c.*331T>G	XP_016859708.1:n.*331T>G
XM_017004220.2:c.*331T>G	XP_016859709.1:n.*331T>G
XR_001738751.2:n.2375T>G
XR_001738752.2:n.2197T>G
XR_427087.4:n.2254T>G
NM_006186.4:c.*331T>G MANE Select	NP_006177.1:n.*331T>G
NM_173173.3:c.*331T>G	NP_775265.1:n.*331T>G