Canonical Allele Identifier: CA10612359

Gene: NR4A2

Linked Data

• ClinVar Variation Id: 331650
• ClinVar RCV Id: RCV000316517
• dbSNP Id: rs563505935
• gnomAD v2: 2-157181323-C-T
• gnomAD v3: 2-156324811-C-T
• gnomAD v4: 2-156324811-C-T
• MyVariant Identifiers: chr2:g.157181323C>T (hg19) ; chr2:g.156324811C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156324811C>T , CM000664.2:g.156324811C>T	GRCh38
NC_000002.11:g.157181323C>T , CM000664.1:g.157181323C>T	GRCh37
NC_000002.10:g.156889569C>T	NCBI36
NG_011821.1:g.12965G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339562.9:c.*933G>A MANE Select	ENSP00000344479.4:n.*933G>A
ENST00000339562.8:c.*933G>A	ENSP00000344479.4:n.*933G>A
NM_006186.3:c.*933G>A	NP_006177.1:n.*933G>A
XM_005246621.2:c.*933G>A	XP_005246678.1:n.*933G>A
XM_005246622.2:c.*933G>A	XP_005246679.1:n.*933G>A
XM_005246623.1:c.*933G>A	XP_005246680.1:n.*933G>A
XM_006712553.2:c.*933G>A	XP_006712616.1:n.*933G>A
XM_011511246.1:c.*964G>A	XP_011509548.1:n.*964G>A
NM_173173.2:c.*933G>A	NP_775265.1:n.*933G>A
XM_005246621.4:c.*933G>A	XP_005246678.1:n.*933G>A
XM_006712553.4:c.*933G>A	XP_006712616.1:n.*933G>A
XM_011511246.2:c.*964G>A	XP_011509548.1:n.*964G>A
XM_017004219.2:c.*933G>A	XP_016859708.1:n.*933G>A
XM_017004220.2:c.*933G>A	XP_016859709.1:n.*933G>A
XR_001738751.2:n.2977G>A
XR_001738752.2:n.2799G>A
XR_427087.4:n.2856G>A
NM_006186.4:c.*933G>A MANE Select	NP_006177.1:n.*933G>A
NM_173173.3:c.*933G>A	NP_775265.1:n.*933G>A