Canonical Allele Identifier: CA2672315348

Gene: NR3C2

Linked Data

• gnomAD v4: 4-148442410-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442410G>T , CM000666.2:g.148442410G>T	GRCh38
NC_000004.11:g.149363562G>T , CM000666.1:g.149363562G>T	GRCh37
NC_000004.10:g.149583012G>T	NCBI36
NG_013350.1:g.5111C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.-253C>A MANE Select	ENSP00000350815.3:n.-253C>A
ENST00000344721.8:c.-3+2116C>A	ENSP00000341390.4:n.-3+2116C>A
ENST00000358102.7:c.-253C>A	ENSP00000350815.3:n.-253C>A
ENST00000625323.2:c.-253C>A	ENSP00000486719.1:n.-253C>A
NM_000901.4:c.-253C>A	NP_000892.2:n.-253C>A
NM_001166104.1:c.-253C>A	NP_001159576.1:n.-253C>A
XM_011531975.1:c.-253C>A	XP_011530277.1:n.-253C>A
XM_011531976.1:c.-3+2116C>A	XP_011530278.1:n.-3+2116C>A
XM_011531977.1:c.-3+2790C>A	XP_011530279.1:n.-3+2790C>A
XM_011531978.1:c.-253C>A	XP_011530280.1:n.-253C>A
NM_001354819.1:c.-3+2116C>A	NP_001341748.1:n.-3+2116C>A
NR_148974.1:n.111C>A
XM_011531978.2:c.-253C>A	XP_011530280.1:n.-253C>A
NM_000901.5:c.-253C>A MANE Select	NP_000892.2:n.-253C>A
NM_001166104.2:c.-253C>A	NP_001159576.1:n.-253C>A
NR_148974.2:n.5C>A