Canonical Allele Identifier: CA358425229

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002526T>A (hg19) ; chr4:g.148081375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081375T>A , CM000666.2:g.148081375T>A	GRCh38
NC_000004.11:g.149002526T>A , CM000666.1:g.149002526T>A	GRCh37
NC_000004.10:g.149221976T>A	NCBI36
NG_013350.1:g.366147A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2924A>T MANE Select	ENSP00000350815.3:p.Asn975Ile
ENST00000342437.8:c.*307A>T	ENSP00000343907.4:n.*307A>T
ENST00000344721.8:c.2924A>T	ENSP00000341390.4:p.Asn975Ile
ENST00000358102.7:c.2924A>T	ENSP00000350815.3:p.Asn975Ile
ENST00000511528.1:c.2936A>T	ENSP00000421481.1:p.Asn979Ile
ENST00000512865.5:c.2573A>T	ENSP00000423510.1:p.Asn858Ile
ENST00000625323.2:c.2936A>T	ENSP00000486719.1:p.Asn979Ile
NM_000901.4:c.2924A>T	NP_000892.2:p.Asn975Ile
NM_001166104.1:c.2573A>T	NP_001159576.1:p.Asn858Ile
XM_011531975.1:c.2936A>T	XP_011530277.1:p.Asn979Ile
XM_011531976.1:c.2936A>T	XP_011530278.1:p.Asn979Ile
XM_011531977.1:c.2936A>T	XP_011530279.1:p.Asn979Ile
NM_001354819.1:c.2573A>T	NP_001341748.1:p.Asn858Ile
NR_148974.1:n.2791A>T
NM_000901.5:c.2924A>T MANE Select	NP_000892.2:p.Asn975Ile
NM_001166104.2:c.2573A>T	NP_001159576.1:p.Asn858Ile
NR_148974.2:n.2685A>T