Canonical Allele Identifier: CA1095738

Gene: RORC

Linked Data

• ClinVar Variation Id: 1626156
• ClinVar RCV Id: RCV002132599
• dbSNP Id: rs372774021
• ExAC: 1:151785700 C / T
• gnomAD v2: 1-151785700-C-T
• MyVariant Identifiers: chr1:g.151785700C>T (hg19) ; chr1:g.151813224C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151813224C>T , CM000663.2:g.151813224C>T	GRCh38
NC_000001.10:g.151785700C>T , CM000663.1:g.151785700C>T	GRCh37
NC_000001.9:g.150052324C>T	NCBI36
NG_029118.1:g.23649G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.889+15G>A	ENSP00000498548.2:n.889+15G>A
ENST00000697811.1:c.933+1350G>A	ENSP00000513447.1:n.933+1350G>A
ENST00000697812.1:n.312+15G>A
ENST00000697813.1:n.1184G>A
ENST00000318247.7:c.1174+15G>A MANE Select	ENSP00000327025.6:n.1174+15G>A
ENST00000356728.11:c.1111+15G>A	ENSP00000349164.6:n.1111+15G>A
ENST00000638901.1:c.1365+15G>A
ENST00000651814.1:c.*131+15G>A	ENSP00000498691.1:n.*131+15G>A
ENST00000651893.1:c.451+15G>A
ENST00000318247.6:c.1174+15G>A	ENSP00000327025.6:n.1174+15G>A
ENST00000356728.10:c.1111+15G>A	ENSP00000349164.6:n.1111+15G>A
ENST00000480719.1:n.1566G>A
NM_001001523.1:c.1111+15G>A	NP_001001523.1:n.1111+15G>A
NM_005060.3:c.1174+15G>A	NP_005051.2:n.1174+15G>A
XM_006711484.2:c.1573+15G>A	XP_006711547.2:n.1573+15G>A
XR_426792.2:n.1935+15G>A
XM_006711484.4:c.1573+15G>A	XP_006711547.2:n.1573+15G>A
NM_005060.4:c.1174+15G>A MANE Select	NP_005051.2:n.1174+15G>A
NM_001001523.2:c.1111+15G>A	NP_001001523.1:n.1111+15G>A