Canonical Allele Identifier: CA358425534

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002584A>G (hg19) ; chr4:g.148081433A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081433A>G , CM000666.2:g.148081433A>G	GRCh38
NC_000004.11:g.149002584A>G , CM000666.1:g.149002584A>G	GRCh37
NC_000004.10:g.149222034A>G	NCBI36
NG_013350.1:g.366089T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2866T>C MANE Select	ENSP00000350815.3:p.Phe956Leu
ENST00000342437.8:c.*249T>C	ENSP00000343907.4:n.*249T>C
ENST00000344721.8:c.2866T>C	ENSP00000341390.4:p.Phe956Leu
ENST00000358102.7:c.2866T>C	ENSP00000350815.3:p.Phe956Leu
ENST00000511528.1:c.2878T>C	ENSP00000421481.1:p.Phe960Leu
ENST00000512865.5:c.2515T>C	ENSP00000423510.1:p.Phe839Leu
ENST00000625323.2:c.2878T>C	ENSP00000486719.1:p.Phe960Leu
NM_000901.4:c.2866T>C	NP_000892.2:p.Phe956Leu
NM_001166104.1:c.2515T>C	NP_001159576.1:p.Phe839Leu
XM_011531975.1:c.2878T>C	XP_011530277.1:p.Phe960Leu
XM_011531976.1:c.2878T>C	XP_011530278.1:p.Phe960Leu
XM_011531977.1:c.2878T>C	XP_011530279.1:p.Phe960Leu
NM_001354819.1:c.2515T>C	NP_001341748.1:p.Phe839Leu
NR_148974.1:n.2733T>C
NM_000901.5:c.2866T>C MANE Select	NP_000892.2:p.Phe956Leu
NM_001166104.2:c.2515T>C	NP_001159576.1:p.Phe839Leu
NR_148974.2:n.2627T>C