Canonical Allele Identifier: CA358425407

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149073627A>C (hg19) ; chr4:g.148152476A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152476A>C , CM000666.2:g.148152476A>C	GRCh38
NC_000004.11:g.149073627A>C , CM000666.1:g.149073627A>C	GRCh37
NC_000004.10:g.149293077A>C	NCBI36
NG_013350.1:g.295046T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2503T>G MANE Select	ENSP00000350815.3:p.Phe835Val
ENST00000342437.8:c.2015-32188T>G	ENSP00000343907.4:n.2015-32188T>G
ENST00000344721.8:c.2503T>G	ENSP00000341390.4:p.Phe835Val
ENST00000358102.7:c.2503T>G	ENSP00000350815.3:p.Phe835Val
ENST00000503174.1:n.432T>G
ENST00000503313.1:n.700T>G
ENST00000511528.1:c.2515T>G	ENSP00000421481.1:p.Phe839Val
ENST00000512865.5:c.2152T>G	ENSP00000423510.1:p.Phe718Val
ENST00000625323.2:c.2515T>G	ENSP00000486719.1:p.Phe839Val
NM_000901.4:c.2503T>G	NP_000892.2:p.Phe835Val
NM_001166104.1:c.2152T>G	NP_001159576.1:p.Phe718Val
XM_011531975.1:c.2515T>G	XP_011530277.1:p.Phe839Val
XM_011531976.1:c.2515T>G	XP_011530278.1:p.Phe839Val
XM_011531977.1:c.2515T>G	XP_011530279.1:p.Phe839Val
XM_011531978.1:c.2515T>G	XP_011530280.1:p.Phe839Val
NM_001354819.1:c.2152T>G	NP_001341748.1:p.Phe718Val
NR_148974.1:n.2378-32188T>G
XM_011531978.2:c.2515T>G	XP_011530280.1:p.Phe839Val
NM_000901.5:c.2503T>G MANE Select	NP_000892.2:p.Phe835Val
NM_001166104.2:c.2152T>G	NP_001159576.1:p.Phe718Val
NR_148974.2:n.2272-32188T>G