Canonical Allele Identifier: CA358425222

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002523G>A (hg19) ; chr4:g.148081372G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081372G>A , CM000666.2:g.148081372G>A	GRCh38
NC_000004.11:g.149002523G>A , CM000666.1:g.149002523G>A	GRCh37
NC_000004.10:g.149221973G>A	NCBI36
NG_013350.1:g.366150C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2927C>T MANE Select	ENSP00000350815.3:p.Ala976Val
ENST00000342437.8:c.*310C>T	ENSP00000343907.4:n.*310C>T
ENST00000344721.8:c.2927C>T	ENSP00000341390.4:p.Ala976Val
ENST00000358102.7:c.2927C>T	ENSP00000350815.3:p.Ala976Val
ENST00000511528.1:c.2939C>T	ENSP00000421481.1:p.Ala980Val
ENST00000512865.5:c.2576C>T	ENSP00000423510.1:p.Ala859Val
ENST00000625323.2:c.2939C>T	ENSP00000486719.1:p.Ala980Val
NM_000901.4:c.2927C>T	NP_000892.2:p.Ala976Val
NM_001166104.1:c.2576C>T	NP_001159576.1:p.Ala859Val
XM_011531975.1:c.2939C>T	XP_011530277.1:p.Ala980Val
XM_011531976.1:c.2939C>T	XP_011530278.1:p.Ala980Val
XM_011531977.1:c.2939C>T	XP_011530279.1:p.Ala980Val
NM_001354819.1:c.2576C>T	NP_001341748.1:p.Ala859Val
NR_148974.1:n.2794C>T
NM_000901.5:c.2927C>T MANE Select	NP_000892.2:p.Ala976Val
NM_001166104.2:c.2576C>T	NP_001159576.1:p.Ala859Val
NR_148974.2:n.2688C>T