Canonical Allele Identifier: CA230620

Gene: CX3CR1

Linked Data

• ClinVar Variation Id: 120091
• ClinVar RCV Id: RCV000106289
• dbSNP Id: rs137854870
• MyVariant Identifiers: chr3:g.39307216A>G (hg19) ; chr3:g.39265725A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265725A>G , CM000665.2:g.39265725A>G	GRCh38
NC_000003.11:g.39307216A>G , CM000665.1:g.39307216A>G	GRCh37
NC_000003.10:g.39282220A>G	NCBI36
NG_016362.1:g.21011T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.785T>C MANE Select	ENSP00000382166.3:p.Phe262Ser
ENST00000358309.3:c.881T>C	ENSP00000351059.3:p.Phe294Ser
ENST00000399220.2:c.785T>C	ENSP00000382166.2:p.Phe262Ser
ENST00000541347.5:c.785T>C	ENSP00000439140.1:p.Phe262Ser
ENST00000542107.5:c.785T>C	ENSP00000444928.1:p.Phe262Ser
NM_001171171.1:c.785T>C	NP_001164642.1:p.Phe262Ser
NM_001171172.1:c.785T>C	NP_001164643.1:p.Phe262Ser
NM_001171174.1:c.881T>C	NP_001164645.1:p.Phe294Ser
NM_001337.3:c.785T>C	NP_001328.1:p.Phe262Ser
NM_001337.4:c.785T>C MANE Select	NP_001328.1:p.Phe262Ser
NM_001171171.2:c.785T>C	NP_001164642.1:p.Phe262Ser
NM_001171172.2:c.785T>C	NP_001164643.1:p.Phe262Ser