Canonical Allele Identifier: CA342013238

Gene: RORC

Linked Data

• ClinVar Variation Id: 1068314
• ClinVar RCV Id: RCV001379824
• dbSNP Id: rs2101656625
• MyVariant Identifiers: chr1:g.151786097C>T (hg19) ; chr1:g.151813621C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151813621C>T , CM000663.2:g.151813621C>T	GRCh38
NC_000001.10:g.151786097C>T , CM000663.1:g.151786097C>T	GRCh37
NC_000001.9:g.150052721C>T	NCBI36
NG_029118.1:g.23252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.649-1G>A	ENSP00000498548.2:n.649-1G>A
ENST00000697811.1:c.933+953G>A	ENSP00000513447.1:n.933+953G>A
ENST00000697812.1:n.72-1G>A
ENST00000697813.1:n.929-1G>A
ENST00000318247.7:c.934-1G>A MANE Select	ENSP00000327025.6:n.934-1G>A
ENST00000356728.11:c.871-1G>A	ENSP00000349164.6:n.871-1G>A
ENST00000638901.1:c.1125-1G>A
ENST00000651814.1:c.1015G>A	ENSP00000498691.1:p.Val339Ile
ENST00000651893.1:c.344-275G>A
ENST00000318247.6:c.934-1G>A	ENSP00000327025.6:n.934-1G>A
ENST00000356728.10:c.871-1G>A	ENSP00000349164.6:n.871-1G>A
ENST00000480719.1:n.1169G>A
NM_001001523.1:c.871-1G>A	NP_001001523.1:n.871-1G>A
NM_005060.3:c.934-1G>A	NP_005051.2:n.934-1G>A
XM_006711484.2:c.1333-1G>A	XP_006711547.2:n.1333-1G>A
XR_426792.2:n.1694G>A
XM_006711484.4:c.1333-1G>A	XP_006711547.2:n.1333-1G>A
NM_005060.4:c.934-1G>A MANE Select	NP_005051.2:n.934-1G>A
NM_001001523.2:c.871-1G>A	NP_001001523.1:n.871-1G>A