Canonical Allele Identifier: CA897898262

Gene: NR1I2

Linked Data

• dbSNP Id: rs1185137012
• gnomAD v3: 3-119817661-T-C
• gnomAD v4: 3-119817661-T-C
• MyVariant Identifiers: chr3:g.119536508T>C (hg19) ; chr3:g.119817661T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119817661T>C , CM000665.2:g.119817661T>C	GRCh38
NC_000003.11:g.119536508T>C , CM000665.1:g.119536508T>C	GRCh37
NC_000003.10:g.121019198T>C	NCBI36
NG_011856.1:g.42178T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.*449T>C MANE Select	ENSP00000377319.3:n.*449T>C
ENST00000466380.6:c.*449T>C	ENSP00000420297.2:n.*449T>C
ENST00000337940.4:c.*449T>C	ENSP00000336528.4:n.*449T>C
ENST00000393716.6:c.*449T>C	ENSP00000377319.2:n.*449T>C
ENST00000466380.5:c.*449T>C	ENSP00000420297.1:n.*449T>C
ENST00000493757.1:n.1886T>C
NM_003889.3:c.*449T>C	NP_003880.3:n.*449T>C
NM_022002.2:c.*449T>C	NP_071285.1:n.*449T>C
NM_033013.2:c.*449T>C	NP_148934.1:n.*449T>C
NM_003889.4:c.*449T>C MANE Select	NP_003880.3:n.*449T>C
NM_022002.3:c.*449T>C	NP_071285.1:n.*449T>C
NM_033013.3:c.*449T>C	NP_148934.1:n.*449T>C