Canonical Allele Identifier: CA2557733

Gene: NR1I2

Linked Data

• dbSNP Id: rs140189458
• ExAC: 3:119526202 C / T
• gnomAD v2: 3-119526202-C-T
• gnomAD v3: 3-119807355-C-T
• gnomAD v4: 3-119807355-C-T
• MyVariant Identifiers: chr3:g.119526202C>T (hg19) ; chr3:g.119807355C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119807355C>T , CM000665.2:g.119807355C>T	GRCh38
NC_000003.11:g.119526202C>T , CM000665.1:g.119526202C>T	GRCh37
NC_000003.10:g.121008892C>T	NCBI36
NG_011856.1:g.31872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393716.8:c.105C>T MANE Select	ENSP00000377319.3:p.Val35=
ENST00000466380.6:c.105C>T	ENSP00000420297.2:p.Val35=
ENST00000648112.1:c.*128C>T	ENSP00000497876.1:n.*128C>T
ENST00000337940.4:c.222C>T	ENSP00000336528.4:p.Val74=
ENST00000393716.6:c.105C>T	ENSP00000377319.2:p.Val35=
ENST00000466380.5:c.105C>T	ENSP00000420297.1:p.Val35=
ENST00000474090.1:n.393C>T
NM_003889.3:c.105C>T	NP_003880.3:p.Val35=
NM_022002.2:c.222C>T	NP_071285.1:p.Val74=
NM_033013.2:c.105C>T	NP_148934.1:p.Val35=
NM_003889.4:c.105C>T MANE Select	NP_003880.3:p.Val35=
NM_022002.3:c.222C>T	NP_071285.1:p.Val74=
NM_033013.3:c.105C>T	NP_148934.1:p.Val35=