Canonical Allele Identifier: CA589562340

Gene: NR4A3

Linked Data

• dbSNP Id: rs1382861027
• gnomAD v2: 9-102589696-A-G
• gnomAD v3: 9-99827414-A-G
• gnomAD v4: 9-99827414-A-G
• MyVariant Identifiers: chr9:g.102589696A>G (hg19) ; chr9:g.99827414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99827414A>G , CM000671.2:g.99827414A>G	GRCh38
NC_000009.11:g.102589696A>G , CM000671.1:g.102589696A>G	GRCh37
NC_000009.10:g.101629517A>G	NCBI36
NG_028910.1:g.10560A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395097.7:c.-2-627A>G MANE Select	ENSP00000378531.2:n.-2-627A>G
ENST00000330847.1:c.31+613A>G	ENSP00000333122.1:n.31+613A>G
ENST00000338488.8:c.-2-627A>G	ENSP00000340301.4:n.-2-627A>G
ENST00000395097.6:c.-2-627A>G	ENSP00000378531.2:n.-2-627A>G
ENST00000618101.4:c.31+613A>G	ENSP00000482027.1:n.31+613A>G
NM_006981.3:c.-2-627A>G	NP_008912.2:n.-2-627A>G
NM_173199.2:c.-2-627A>G	NP_775291.1:n.-2-627A>G
NM_173200.2:c.31+613A>G	NP_775292.1:n.31+613A>G
XM_005252237.2:c.31+613A>G	XP_005252294.1:n.31+613A>G
XM_011519048.1:c.-55A>G	XP_011517350.1:n.-55A>G
XM_011519049.1:c.-55A>G	XP_011517351.1:n.-55A>G
XM_017015162.1:c.-55A>G	XP_016870651.1:n.-55A>G
NM_006981.4:c.-2-627A>G MANE Select	NP_008912.2:n.-2-627A>G
NM_173199.3:c.-2-627A>G	NP_775291.1:n.-2-627A>G
NM_173199.4:c.-2-627A>G	NP_775291.1:n.-2-627A>G
NM_173200.3:c.31+613A>G	NP_775292.1:n.31+613A>G