Canonical Allele Identifier: CA352201810

Gene: CX3CR1

Linked Data

• dbSNP Id: rs1243086133
• gnomAD v3: 3-39265891-T-C
• gnomAD v4: 3-39265891-T-C
• MyVariant Identifiers: chr3:g.39307382T>C (hg19) ; chr3:g.39265891T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265891T>C , CM000665.2:g.39265891T>C	GRCh38
NC_000003.11:g.39307382T>C , CM000665.1:g.39307382T>C	GRCh37
NC_000003.10:g.39282386T>C	NCBI36
NG_016362.1:g.20845A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.619A>G MANE Select	ENSP00000382166.3:p.Met207Val
ENST00000358309.3:c.715A>G	ENSP00000351059.3:p.Met239Val
ENST00000399220.2:c.619A>G	ENSP00000382166.2:p.Met207Val
ENST00000541347.5:c.619A>G	ENSP00000439140.1:p.Met207Val
ENST00000542107.5:c.619A>G	ENSP00000444928.1:p.Met207Val
NM_001171171.1:c.619A>G	NP_001164642.1:p.Met207Val
NM_001171172.1:c.619A>G	NP_001164643.1:p.Met207Val
NM_001171174.1:c.715A>G	NP_001164645.1:p.Met239Val
NM_001337.3:c.619A>G	NP_001328.1:p.Met207Val
NM_001337.4:c.619A>G MANE Select	NP_001328.1:p.Met207Val
NM_001171171.2:c.619A>G	NP_001164642.1:p.Met207Val
NM_001171172.2:c.619A>G	NP_001164643.1:p.Met207Val