Canonical Allele Identifier: CA2839789233

Gene: NR3C2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081312C>A , CM000666.2:g.148081312C>A	GRCh38
NC_000004.11:g.149002463C>A , CM000666.1:g.149002463C>A	GRCh37
NC_000004.10:g.149221913C>A	NCBI36
NG_013350.1:g.366210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.*32G>T MANE Select	ENSP00000350815.3:n.*32G>T
ENST00000342437.8:c.*370G>T	ENSP00000343907.4:n.*370G>T
ENST00000344721.8:c.*32G>T	ENSP00000341390.4:n.*32G>T
ENST00000358102.7:c.*32G>T	ENSP00000350815.3:n.*32G>T
ENST00000512865.5:c.*32G>T	ENSP00000423510.1:n.*32G>T
ENST00000625323.2:c.*32G>T	ENSP00000486719.1:n.*32G>T
NM_000901.4:c.*32G>T	NP_000892.2:n.*32G>T
NM_001166104.1:c.*32G>T	NP_001159576.1:n.*32G>T
XM_011531975.1:c.*32G>T	XP_011530277.1:n.*32G>T
XM_011531976.1:c.*32G>T	XP_011530278.1:n.*32G>T
XM_011531977.1:c.*32G>T	XP_011530279.1:n.*32G>T
NM_001354819.1:c.*32G>T	NP_001341748.1:n.*32G>T
NR_148974.1:n.2854G>T
NM_000901.5:c.*32G>T MANE Select	NP_000892.2:n.*32G>T
NM_001166104.2:c.*32G>T	NP_001159576.1:n.*32G>T
NR_148974.2:n.2748G>T