Canonical Allele Identifier: CA555538968

Gene: NR3C2

Linked Data

• dbSNP Id: rs1201811365
• gnomAD v2: 4-149002416-A-AAAC
• gnomAD v3: 4-148081265-A-AAAC
• gnomAD v4: 4-148081265-A-AAAC
• MyVariant Identifiers: chr4:g.149002416_149002417insAAC (hg19) ; chr4:g.148081265_148081266insAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081267_148081269dup , CM000666.2:g.148081267_148081269dup	GRCh38
NC_000004.11:g.149002418_149002420dup , CM000666.1:g.149002418_149002420dup	GRCh37
NC_000004.10:g.149221868_149221870dup	NCBI36
NG_013350.1:g.366254_366256dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.*76_*78dup MANE Select	ENSP00000350815.3:n.*76_*78dup
ENST00000342437.8:c.*414_*416dup	ENSP00000343907.4:n.*414_*416dup
ENST00000344721.8:c.*76_*78dup	ENSP00000341390.4:n.*76_*78dup
ENST00000358102.7:c.*76_*78dup	ENSP00000350815.3:n.*76_*78dup
ENST00000512865.5:c.*76_*78dup	ENSP00000423510.1:n.*76_*78dup
ENST00000625323.2:c.*76_*78dup	ENSP00000486719.1:n.*76_*78dup
NM_000901.4:c.*76_*78dup	NP_000892.2:n.*76_*78dup
NM_001166104.1:c.*76_*78dup	NP_001159576.1:n.*76_*78dup
XM_011531975.1:c.*76_*78dup	XP_011530277.1:n.*76_*78dup
XM_011531976.1:c.*76_*78dup	XP_011530278.1:n.*76_*78dup
XM_011531977.1:c.*76_*78dup	XP_011530279.1:n.*76_*78dup
NM_001354819.1:c.*76_*78dup	NP_001341748.1:n.*76_*78dup
NR_148974.1:n.2898_2900dup
NM_000901.5:c.*76_*78dup MANE Select	NP_000892.2:n.*76_*78dup
NM_001166104.2:c.*76_*78dup	NP_001159576.1:n.*76_*78dup
NR_148974.2:n.2792_2794dup