Canonical Allele Identifier: CA348681784

Gene: NR4A2

Linked Data

• gnomAD v4: 2-156329446-C-G
• MyVariant Identifiers: chr2:g.157185958C>G (hg19) ; chr2:g.156329446C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.156329446C>G , CM000664.2:g.156329446C>G	GRCh38
NC_000002.11:g.157185958C>G , CM000664.1:g.157185958C>G	GRCh37
NC_000002.10:g.156894204C>G	NCBI36
NG_011821.1:g.8330G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700228.1:c.612G>C	ENSP00000514865.1:p.Gln204His
ENST00000700230.1:c.174G>C	ENSP00000514867.1:p.Gln58His
ENST00000700231.1:c.741G>C	ENSP00000514868.1:p.Gln247His
ENST00000339562.9:c.741G>C MANE Select	ENSP00000344479.4:p.Gln247His
ENST00000675870.1:c.552G>C	ENSP00000502739.1:p.Gln184His
ENST00000339562.8:c.741G>C	ENSP00000344479.4:p.Gln247His
ENST00000406048.2:c.208+468G>C
ENST00000409108.6:c.741G>C	ENSP00000386993.2:p.Gln247His
ENST00000409572.5:c.741G>C	ENSP00000386747.1:p.Gln247His
ENST00000417764.5:c.552G>C	ENSP00000415632.1:p.Gln184His
ENST00000417972.5:c.552G>C	ENSP00000394671.1:p.Gln184His
ENST00000424077.1:c.741G>C	ENSP00000406808.1:p.Gln247His
ENST00000426264.5:c.552G>C	ENSP00000389986.1:p.Gln184His
ENST00000429376.5:c.552G>C	ENSP00000410952.1:p.Gln184His
NM_006186.3:c.741G>C	NP_006177.1:p.Gln247His
XM_005246621.2:c.774G>C	XP_005246678.1:p.Gln258His
XM_005246622.2:c.552G>C	XP_005246679.1:p.Gln184His
XM_005246623.1:c.552G>C	XP_005246680.1:p.Gln184His
XM_006712553.2:c.774G>C	XP_006712616.1:p.Gln258His
XM_011511246.1:c.774G>C	XP_011509548.1:p.Gln258His
XR_427087.2:n.2947G>C
NM_173173.2:c.552G>C	NP_775265.1:p.Gln184His
XM_005246621.4:c.774G>C	XP_005246678.1:p.Gln258His
XM_006712553.4:c.774G>C	XP_006712616.1:p.Gln258His
XM_011511246.2:c.774G>C	XP_011509548.1:p.Gln258His
XM_017004219.2:c.741G>C	XP_016859708.1:p.Gln247His
XM_017004220.2:c.741G>C	XP_016859709.1:p.Gln247His
XR_001738751.2:n.1109G>C
XR_001738752.2:n.931G>C
XR_427087.4:n.988G>C
NM_006186.4:c.741G>C MANE Select	NP_006177.1:p.Gln247His
NM_173173.3:c.552G>C	NP_775265.1:p.Gln184His