Canonical Allele Identifier: CA383798912

Gene: C3AR1

Linked Data

• MyVariant Identifiers: chr12:g.8212331A>C (hg19) ; chr12:g.8059735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8059735A>C , CM000674.2:g.8059735A>C	GRCh38
NC_000012.11:g.8212331A>C , CM000674.1:g.8212331A>C	GRCh37
NC_000012.10:g.8103598A>C	NCBI36
NG_050736.1:g.11737T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307637.5:c.451T>G MANE Select	ENSP00000302079.4:p.Phe151Val
ENST00000307637.4:c.451T>G	ENSP00000302079.4:p.Phe151Val
NM_004054.2:c.451T>G	NP_004045.1:p.Phe151Val
NM_001326475.1:c.451T>G	NP_001313404.1:p.Phe151Val
NM_001326477.1:c.451T>G	NP_001313406.1:p.Phe151Val
NM_004054.3:c.451T>G	NP_004045.1:p.Phe151Val
NM_001326475.2:c.451T>G	NP_001313404.1:p.Phe151Val
NM_001326477.2:c.451T>G	NP_001313406.1:p.Phe151Val
NM_004054.4:c.451T>G MANE Select	NP_004045.1:p.Phe151Val