Canonical Allele Identifier: CA107877833

Gene: NR3C2

Linked Data

• dbSNP Id: rs72646915
• gnomAD v2: 4-149363640-G-C
• gnomAD v3: 4-148442488-G-C
• gnomAD v4: 4-148442488-G-C
• MyVariant Identifiers: chr4:g.149363640G>C (hg19) ; chr4:g.148442488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148442488G>C , CM000666.2:g.148442488G>C	GRCh38
NC_000004.11:g.149363640G>C , CM000666.1:g.149363640G>C	GRCh37
NC_000004.10:g.149583090G>C	NCBI36
NG_013350.1:g.5033C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344721.8:c.-3+2038C>G	ENSP00000341390.4:n.-3+2038C>G
ENST00000358102.7:c.-331C>G	ENSP00000350815.3:n.-331C>G
ENST00000625323.2:c.-331C>G	ENSP00000486719.1:n.-331C>G
NM_000901.4:c.-331C>G	NP_000892.2:n.-331C>G
NM_001166104.1:c.-331C>G	NP_001159576.1:n.-331C>G
XM_011531975.1:c.-331C>G	XP_011530277.1:n.-331C>G
XM_011531976.1:c.-3+2038C>G	XP_011530278.1:n.-3+2038C>G
XM_011531977.1:c.-3+2712C>G	XP_011530279.1:n.-3+2712C>G
XM_011531978.1:c.-331C>G	XP_011530280.1:n.-331C>G
NM_001354819.1:c.-3+2038C>G	NP_001341748.1:n.-3+2038C>G
NR_148974.1:n.33C>G
XM_011531978.2:c.-331C>G	XP_011530280.1:n.-331C>G