Canonical Allele Identifier: CA869232317

Gene: NR4A3

Linked Data

• dbSNP Id: rs1295467461
• gnomAD v3: 9-99827454-G-T
• gnomAD v4: 9-99827454-G-T
• MyVariant Identifiers: chr9:g.102589736G>T (hg19) ; chr9:g.99827454G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99827454G>T , CM000671.2:g.99827454G>T	GRCh38
NC_000009.11:g.102589736G>T , CM000671.1:g.102589736G>T	GRCh37
NC_000009.10:g.101629557G>T	NCBI36
NG_028910.1:g.10600G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395097.7:c.-2-587G>T MANE Select	ENSP00000378531.2:n.-2-587G>T
ENST00000330847.1:c.32-587G>T	ENSP00000333122.1:n.32-587G>T
ENST00000338488.8:c.-2-587G>T	ENSP00000340301.4:n.-2-587G>T
ENST00000395097.6:c.-2-587G>T	ENSP00000378531.2:n.-2-587G>T
ENST00000618101.4:c.32-587G>T	ENSP00000482027.1:n.32-587G>T
NM_006981.3:c.-2-587G>T	NP_008912.2:n.-2-587G>T
NM_173199.2:c.-2-587G>T	NP_775291.1:n.-2-587G>T
NM_173200.2:c.32-587G>T	NP_775292.1:n.32-587G>T
XM_005252237.2:c.32-587G>T	XP_005252294.1:n.32-587G>T
XM_011519048.1:c.-15G>T	XP_011517350.1:n.-15G>T
XM_011519049.1:c.-15G>T	XP_011517351.1:n.-15G>T
XM_017015162.1:c.-15G>T	XP_016870651.1:n.-15G>T
NM_006981.4:c.-2-587G>T MANE Select	NP_008912.2:n.-2-587G>T
NM_173199.3:c.-2-587G>T	NP_775291.1:n.-2-587G>T
NM_173199.4:c.-2-587G>T	NP_775291.1:n.-2-587G>T
NM_173200.3:c.32-587G>T	NP_775292.1:n.32-587G>T