Canonical Allele Identifier: CA441753929

Gene: NR3C2

Linked Data

• MyVariant Identifiers: chr4:g.149002531C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148081380C>G , CM000666.2:g.148081380C>G	GRCh38
NC_000004.11:g.149002531C>G , CM000666.1:g.149002531C>G	GRCh37
NC_000004.10:g.149221981C>G	NCBI36
NG_013350.1:g.366142G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358102.8:c.2919G>C MANE Select	ENSP00000350815.3:p.Ser973=
ENST00000342437.8:c.*302G>C	ENSP00000343907.4:n.*302G>C
ENST00000344721.8:c.2919G>C	ENSP00000341390.4:p.Ser973=
ENST00000358102.7:c.2919G>C	ENSP00000350815.3:p.Ser973=
ENST00000511528.1:c.2931G>C	ENSP00000421481.1:p.Ser977=
ENST00000512865.5:c.2568G>C	ENSP00000423510.1:p.Ser856=
ENST00000625323.2:c.2931G>C	ENSP00000486719.1:p.Ser977=
NM_000901.4:c.2919G>C	NP_000892.2:p.Ser973=
NM_001166104.1:c.2568G>C	NP_001159576.1:p.Ser856=
XM_011531975.1:c.2931G>C	XP_011530277.1:p.Ser977=
XM_011531976.1:c.2931G>C	XP_011530278.1:p.Ser977=
XM_011531977.1:c.2931G>C	XP_011530279.1:p.Ser977=
NM_001354819.1:c.2568G>C	NP_001341748.1:p.Ser856=
NR_148974.1:n.2786G>C
NM_000901.5:c.2919G>C MANE Select	NP_000892.2:p.Ser973=
NM_001166104.2:c.2568G>C	NP_001159576.1:p.Ser856=
NR_148974.2:n.2680G>C