Canonical Allele Identifier: CA441754528

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149073754G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148152603G>A , CM000666.2:g.148152603G>A	GRCh38
NC_000004.11:g.149073754G>A , CM000666.1:g.149073754G>A	GRCh37
NC_000004.10:g.149293204G>A	NCBI36
NG_013350.1:g.294919C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2376C>T MANE Select	ENSP00000350815.3:p.Asn792=
ENST00000342437.8:c.2015-32315C>T	ENSP00000343907.4:n.2015-32315C>T
ENST00000344721.8:c.2376C>T	ENSP00000341390.4:p.Asn792=
ENST00000358102.7:c.2376C>T	ENSP00000350815.3:p.Asn792=
ENST00000503174.1:n.305C>T
ENST00000503313.1:n.573C>T
ENST00000511528.1:c.2388C>T	ENSP00000421481.1:p.Asn796=
ENST00000512865.5:c.2025C>T	ENSP00000423510.1:p.Asn675=
ENST00000625323.2:c.2388C>T	ENSP00000486719.1:p.Asn796=
NM_000901.4:c.2376C>T	NP_000892.2:p.Asn792=
NM_001166104.1:c.2025C>T	NP_001159576.1:p.Asn675=
XM_011531975.1:c.2388C>T	XP_011530277.1:p.Asn796=
XM_011531976.1:c.2388C>T	XP_011530278.1:p.Asn796=
XM_011531977.1:c.2388C>T	XP_011530279.1:p.Asn796=
XM_011531978.1:c.2388C>T	XP_011530280.1:p.Asn796=
NM_001354819.1:c.2025C>T	NP_001341748.1:p.Asn675=
NR_148974.1:n.2378-32315C>T
XM_011531978.2:c.2388C>T	XP_011530280.1:p.Asn796=
NM_000901.5:c.2376C>T MANE Select	NP_000892.2:p.Asn792=
NM_001166104.2:c.2025C>T	NP_001159576.1:p.Asn675=
NR_148974.2:n.2272-32315C>T