Canonical Allele Identifier: CA358425228

Gene: NR3C2

Linked Data

• dbSNP Id: rs1048114231
• gnomAD v2: 4-149002525-G-T
• gnomAD v3: 4-148081374-G-T
• gnomAD v4: 4-148081374-G-T
• MyVariant Identifiers: chr4:g.149002525G>T (hg19) ; chr4:g.148081374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081374G>T , CM000666.2:g.148081374G>T	GRCh38
NC_000004.11:g.149002525G>T , CM000666.1:g.149002525G>T	GRCh37
NC_000004.10:g.149221975G>T	NCBI36
NG_013350.1:g.366148C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358102.8:c.2925C>A MANE Select	ENSP00000350815.3:p.Asn975Lys
ENST00000342437.8:c.*308C>A	ENSP00000343907.4:n.*308C>A
ENST00000344721.8:c.2925C>A	ENSP00000341390.4:p.Asn975Lys
ENST00000358102.7:c.2925C>A	ENSP00000350815.3:p.Asn975Lys
ENST00000511528.1:c.2937C>A	ENSP00000421481.1:p.Asn979Lys
ENST00000512865.5:c.2574C>A	ENSP00000423510.1:p.Asn858Lys
ENST00000625323.2:c.2937C>A	ENSP00000486719.1:p.Asn979Lys
NM_000901.4:c.2925C>A	NP_000892.2:p.Asn975Lys
NM_001166104.1:c.2574C>A	NP_001159576.1:p.Asn858Lys
XM_011531975.1:c.2937C>A	XP_011530277.1:p.Asn979Lys
XM_011531976.1:c.2937C>A	XP_011530278.1:p.Asn979Lys
XM_011531977.1:c.2937C>A	XP_011530279.1:p.Asn979Lys
NM_001354819.1:c.2574C>A	NP_001341748.1:p.Asn858Lys
NR_148974.1:n.2792C>A
NM_000901.5:c.2925C>A MANE Select	NP_000892.2:p.Asn975Lys
NM_001166104.2:c.2574C>A	NP_001159576.1:p.Asn858Lys
NR_148974.2:n.2686C>A