Canonical Allele Identifier: CA2014392178

Gene: C1R

Linked Data

• dbSNP Id: rs1938156820

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086401A>G , CM000674.2:g.7086401A>G	GRCh38
NG_062465.1:g.11207T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1095T>C MANE Select	ENSP00000497341.1:p.His365=
ENST00000648162.1:n.1067T>C
ENST00000649804.1:c.189T>C	ENSP00000497938.1:p.His63=
ENST00000535233.6:c.993T>C	ENSP00000438636.3:p.His331=
ENST00000536053.6:c.1137T>C	ENSP00000444271.3:p.His379=
ENST00000540394.5:n.2160T>C
ENST00000542285.5:c.1095T>C	ENSP00000438615.2:p.His365=
ENST00000602298.2:n.1444T>C
NM_001733.4:c.1095T>C	NP_001724.3:p.His365=
NM_001354346.1:c.1137T>C	NP_001341275.1:p.His379=
NM_001733.6:c.1095T>C	NP_001724.4:p.His365=
NM_001733.7:c.1095T>C MANE Select	NP_001724.4:p.His365=
NM_001354346.2:c.1137T>C	NP_001341275.1:p.His379=