Canonical Allele Identifier: CA2838197039

Gene: RORC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151816629A>G , CM000663.2:g.151816629A>G	GRCh38
NC_000001.10:g.151789105A>G , CM000663.1:g.151789105A>G	GRCh37
NC_000001.9:g.150055729A>G	NCBI36
NG_029118.1:g.20244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652040.2:c.13+35T>C	ENSP00000498548.2:n.13+35T>C
ENST00000697811.1:c.298+35T>C	ENSP00000513447.1:n.298+35T>C
ENST00000697813.1:n.293+35T>C
ENST00000318247.7:c.298+35T>C MANE Select	ENSP00000327025.6:n.298+35T>C
ENST00000356728.11:c.235+35T>C	ENSP00000349164.6:n.235+35T>C
ENST00000638901.1:c.489+35T>C
ENST00000651025.1:n.412T>C
ENST00000651814.1:c.298+35T>C	ENSP00000498691.1:n.298+35T>C
ENST00000652040.1:c.13+35T>C	ENSP00000498548.1:n.13+35T>C
ENST00000318247.6:c.298+35T>C	ENSP00000327025.6:n.298+35T>C
ENST00000356728.10:c.235+35T>C	ENSP00000349164.6:n.235+35T>C
NM_001001523.1:c.235+35T>C	NP_001001523.1:n.235+35T>C
NM_005060.3:c.298+35T>C	NP_005051.2:n.298+35T>C
XM_006711484.2:c.697+35T>C	XP_006711547.2:n.697+35T>C
XR_426792.2:n.977+35T>C
XM_006711484.4:c.697+35T>C	XP_006711547.2:n.697+35T>C
NM_005060.4:c.298+35T>C MANE Select	NP_005051.2:n.298+35T>C
NM_001001523.2:c.235+35T>C	NP_001001523.1:n.235+35T>C