Canonical Allele Identifier: CA869232273

Gene: NR4A3

Linked Data

• dbSNP Id: rs1408197365
• MyVariant Identifiers: chr9:g.102589665T>C (hg19) ; chr9:g.99827383T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99827383T>C , CM000671.2:g.99827383T>C	GRCh38
NC_000009.11:g.102589665T>C , CM000671.1:g.102589665T>C	GRCh37
NC_000009.10:g.101629486T>C	NCBI36
NG_028910.1:g.10529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395097.7:c.-2-658T>C MANE Select	ENSP00000378531.2:n.-2-658T>C
ENST00000330847.1:c.31+582T>C	ENSP00000333122.1:n.31+582T>C
ENST00000338488.8:c.-2-658T>C	ENSP00000340301.4:n.-2-658T>C
ENST00000395097.6:c.-2-658T>C	ENSP00000378531.2:n.-2-658T>C
ENST00000618101.4:c.31+582T>C	ENSP00000482027.1:n.31+582T>C
NM_006981.3:c.-2-658T>C	NP_008912.2:n.-2-658T>C
NM_173199.2:c.-2-658T>C	NP_775291.1:n.-2-658T>C
NM_173200.2:c.31+582T>C	NP_775292.1:n.31+582T>C
XM_005252237.2:c.31+582T>C	XP_005252294.1:n.31+582T>C
XM_011519048.1:c.-86T>C	XP_011517350.1:n.-86T>C
XM_011519049.1:c.-86T>C	XP_011517351.1:n.-86T>C
XM_017015162.1:c.-86T>C	XP_016870651.1:n.-86T>C
NM_006981.4:c.-2-658T>C MANE Select	NP_008912.2:n.-2-658T>C
NM_173199.3:c.-2-658T>C	NP_775291.1:n.-2-658T>C
NM_173199.4:c.-2-658T>C	NP_775291.1:n.-2-658T>C
NM_173200.3:c.31+582T>C	NP_775292.1:n.31+582T>C