Canonical Allele Identifier: CA1502460751

Gene: NR3C2

Linked Data

• dbSNP Id: rs1750109691
• gnomAD v4: 4-148436882-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148436888dup , CM000666.2:g.148436888dup	GRCh38
NC_000004.11:g.149358040dup , CM000666.1:g.149358040dup	GRCh37
NC_000004.10:g.149577490dup	NCBI36
NG_013350.1:g.10638dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.-2-21dup MANE Select	ENSP00000350815.3:n.-2-21dup
ENST00000342437.8:c.-2-21dup	ENSP00000343907.4:n.-2-21dup
ENST00000344721.8:c.-2-21dup	ENSP00000341390.4:n.-2-21dup
ENST00000358102.7:c.-2-21dup	ENSP00000350815.3:n.-2-21dup
ENST00000512865.5:c.-2-21dup	ENSP00000423510.1:n.-2-21dup
ENST00000625323.2:c.-2-21dup	ENSP00000486719.1:n.-2-21dup
NM_000901.4:c.-2-21dup	NP_000892.2:n.-2-21dup
NM_001166104.1:c.-2-21dup	NP_001159576.1:n.-2-21dup
XM_011531975.1:c.-2-21dup	XP_011530277.1:n.-2-21dup
XM_011531976.1:c.-2-21dup	XP_011530278.1:n.-2-21dup
XM_011531977.1:c.-2-21dup	XP_011530279.1:n.-2-21dup
XM_011531978.1:c.-2-21dup	XP_011530280.1:n.-2-21dup
NM_001354819.1:c.-2-21dup	NP_001341748.1:n.-2-21dup
NR_148974.1:n.362-21dup
XM_011531978.2:c.-2-21dup	XP_011530280.1:n.-2-21dup
NM_000901.5:c.-2-21dup MANE Select	NP_000892.2:n.-2-21dup
NM_001166104.2:c.-2-21dup	NP_001159576.1:n.-2-21dup
NR_148974.2:n.256-21dup