Canonical Allele Identifier: CA2326909

Gene: CX3CR1

Linked Data

• dbSNP Id: rs771058178
• ExAC: 3:39307279 A / G
• gnomAD v2: 3-39307279-A-G
• gnomAD v3: 3-39265788-A-G
• gnomAD v4: 3-39265788-A-G
• MyVariant Identifiers: chr3:g.39307279A>G (hg19) ; chr3:g.39265788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265788A>G , CM000665.2:g.39265788A>G	GRCh38
NC_000003.11:g.39307279A>G , CM000665.1:g.39307279A>G	GRCh37
NC_000003.10:g.39282283A>G	NCBI36
NG_016362.1:g.20948T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.722T>C MANE Select	ENSP00000382166.3:p.Phe241Ser
ENST00000358309.3:c.818T>C	ENSP00000351059.3:p.Phe273Ser
ENST00000399220.2:c.722T>C	ENSP00000382166.2:p.Phe241Ser
ENST00000541347.5:c.722T>C	ENSP00000439140.1:p.Phe241Ser
ENST00000542107.5:c.722T>C	ENSP00000444928.1:p.Phe241Ser
NM_001171171.1:c.722T>C	NP_001164642.1:p.Phe241Ser
NM_001171172.1:c.722T>C	NP_001164643.1:p.Phe241Ser
NM_001171174.1:c.818T>C	NP_001164645.1:p.Phe273Ser
NM_001337.3:c.722T>C	NP_001328.1:p.Phe241Ser
NM_001337.4:c.722T>C MANE Select	NP_001328.1:p.Phe241Ser
NM_001171171.2:c.722T>C	NP_001164642.1:p.Phe241Ser
NM_001171172.2:c.722T>C	NP_001164643.1:p.Phe241Ser