Canonical Allele Identifier: CA73027592

Gene: CX3CR1

Linked Data

• dbSNP Id: rs752967506
• gnomAD v2: 3-39307070-A-C
• gnomAD v4: 3-39265579-A-C
• MyVariant Identifiers: chr3:g.39307070A>C (hg19) ; chr3:g.39265579A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265579A>C , CM000665.2:g.39265579A>C	GRCh38
NC_000003.11:g.39307070A>C , CM000665.1:g.39307070A>C	GRCh37
NC_000003.10:g.39282074A>C	NCBI36
NG_016362.1:g.21157T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.931T>G MANE Select	ENSP00000382166.3:p.Cys311Gly
ENST00000358309.3:c.1027T>G	ENSP00000351059.3:p.Cys343Gly
ENST00000399220.2:c.931T>G	ENSP00000382166.2:p.Cys311Gly
ENST00000541347.5:c.931T>G	ENSP00000439140.1:p.Cys311Gly
ENST00000542107.5:c.931T>G	ENSP00000444928.1:p.Cys311Gly
NM_001171171.1:c.931T>G	NP_001164642.1:p.Cys311Gly
NM_001171172.1:c.931T>G	NP_001164643.1:p.Cys311Gly
NM_001171174.1:c.1027T>G	NP_001164645.1:p.Cys343Gly
NM_001337.3:c.931T>G	NP_001328.1:p.Cys311Gly
NM_001337.4:c.931T>G MANE Select	NP_001328.1:p.Cys311Gly
NM_001171171.2:c.931T>G	NP_001164642.1:p.Cys311Gly
NM_001171172.2:c.931T>G	NP_001164643.1:p.Cys311Gly