Canonical Allele Identifier: CA1916475

Gene: NR4A2

Linked Data

• dbSNP Id: rs368458999
• ExAC: 2:157186388 C / T
• gnomAD v2: 2-157186388-C-T
• gnomAD v3: 2-156329876-C-T
• gnomAD v4: 2-156329876-C-T
• MyVariant Identifiers: chr2:g.157186388C>T (hg19) ; chr2:g.156329876C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329876C>T , CM000664.2:g.156329876C>T	GRCh38
NC_000002.11:g.157186388C>T , CM000664.1:g.157186388C>T	GRCh37
NC_000002.10:g.156894634C>T	NCBI36
NG_011821.1:g.7900G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421709.2:c.122G>A	ENSP00000388120.2:p.Ser41Asn
ENST00000700228.1:c.182G>A	ENSP00000514865.1:p.Ser61Asn
ENST00000700231.1:c.311G>A	ENSP00000514868.1:p.Ser104Asn
ENST00000339562.9:c.311G>A MANE Select	ENSP00000344479.4:p.Ser104Asn
ENST00000675870.1:c.122G>A	ENSP00000502739.1:p.Ser41Asn
ENST00000339562.8:c.311G>A	ENSP00000344479.4:p.Ser104Asn
ENST00000406048.2:c.208+38G>A
ENST00000409108.6:c.311G>A	ENSP00000386993.2:p.Ser104Asn
ENST00000409572.5:c.311G>A	ENSP00000386747.1:p.Ser104Asn
ENST00000417764.5:c.122G>A	ENSP00000415632.1:p.Ser41Asn
ENST00000417972.5:c.122G>A	ENSP00000394671.1:p.Ser41Asn
ENST00000421709.1:c.122G>A	ENSP00000388120.1:p.Ser41Asn
ENST00000424077.1:c.311G>A	ENSP00000406808.1:p.Ser104Asn
ENST00000426264.5:c.122G>A	ENSP00000389986.1:p.Ser41Asn
ENST00000429376.5:c.122G>A	ENSP00000410952.1:p.Ser41Asn
NM_006186.3:c.311G>A	NP_006177.1:p.Ser104Asn
XM_005246621.2:c.344G>A	XP_005246678.1:p.Ser115Asn
XM_005246622.2:c.122G>A	XP_005246679.1:p.Ser41Asn
XM_005246623.1:c.122G>A	XP_005246680.1:p.Ser41Asn
XM_006712553.2:c.344G>A	XP_006712616.1:p.Ser115Asn
XM_011511246.1:c.344G>A	XP_011509548.1:p.Ser115Asn
XR_427087.2:n.2517G>A
NM_173173.2:c.122G>A	NP_775265.1:p.Ser41Asn
XM_005246621.4:c.344G>A	XP_005246678.1:p.Ser115Asn
XM_006712553.4:c.344G>A	XP_006712616.1:p.Ser115Asn
XM_011511246.2:c.344G>A	XP_011509548.1:p.Ser115Asn
XM_017004219.2:c.311G>A	XP_016859708.1:p.Ser104Asn
XM_017004220.2:c.311G>A	XP_016859709.1:p.Ser104Asn
XR_001738751.2:n.679G>A
XR_001738752.2:n.501G>A
XR_427087.4:n.558G>A
NM_006186.4:c.311G>A MANE Select	NP_006177.1:p.Ser104Asn
NM_173173.3:c.122G>A	NP_775265.1:p.Ser41Asn