Canonical Allele Identifier: CA889362293

Gene: RORC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151829204G>T , CM000663.2:g.151829204G>T	GRCh38
NC_000001.10:g.151801680G>T , CM000663.1:g.151801680G>T	GRCh37
NC_000001.9:g.150068304G>T	NCBI36
NG_029118.1:g.7669C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.-130+225C>A	ENSP00000498548.2:n.-130+225C>A
ENST00000697811.1:c.70+225C>A	ENSP00000513447.1:n.70+225C>A
ENST00000697813.1:n.151+225C>A
ENST00000318247.7:c.70+225C>A MANE Select	ENSP00000327025.6:n.70+225C>A
ENST00000638901.1:c.261+225C>A
ENST00000651814.1:c.70+225C>A	ENSP00000498691.1:n.70+225C>A
ENST00000652040.1:c.-130+225C>A	ENSP00000498548.1:n.-130+225C>A
ENST00000318247.6:c.70+225C>A	ENSP00000327025.6:n.70+225C>A
NM_005060.3:c.70+225C>A	NP_005051.2:n.70+225C>A
XM_006711484.2:c.469+225C>A	XP_006711547.2:n.469+225C>A
XR_426792.2:n.749+225C>A
XM_006711484.4:c.469+225C>A	XP_006711547.2:n.469+225C>A
NM_005060.4:c.70+225C>A MANE Select	NP_005051.2:n.70+225C>A