Canonical Allele Identifier: CA478529269

Gene: C3AR1

Linked Data

• MyVariant Identifiers: chr12:g.8212434A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8059838A>G , CM000674.2:g.8059838A>G	GRCh38
NC_000012.11:g.8212434A>G , CM000674.1:g.8212434A>G	GRCh37
NC_000012.10:g.8103701A>G	NCBI36
NG_050736.1:g.11634T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307637.5:c.348T>C MANE Select	ENSP00000302079.4:p.Ile116=
ENST00000307637.4:c.348T>C	ENSP00000302079.4:p.Ile116=
ENST00000546241.1:c.348T>C	ENSP00000444500.1:p.Ile116=
NM_004054.2:c.348T>C	NP_004045.1:p.Ile116=
NM_001326475.1:c.348T>C	NP_001313404.1:p.Ile116=
NM_001326477.1:c.348T>C	NP_001313406.1:p.Ile116=
NM_004054.3:c.348T>C	NP_004045.1:p.Ile116=
NM_001326475.2:c.348T>C	NP_001313404.1:p.Ile116=
NM_001326477.2:c.348T>C	NP_001313406.1:p.Ile116=
NM_004054.4:c.348T>C MANE Select	NP_004045.1:p.Ile116=