Canonical Allele Identifier: CA352203462

Gene: CX3CR1

Linked Data

• dbSNP Id: rs2040695944
• MyVariant Identifiers: chr3:g.39307610T>C (hg19) ; chr3:g.39266119T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39266119T>C , CM000665.2:g.39266119T>C	GRCh38
NC_000003.11:g.39307610T>C , CM000665.1:g.39307610T>C	GRCh37
NC_000003.10:g.39282614T>C	NCBI36
NG_016362.1:g.20617A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.391A>G MANE Select	ENSP00000382166.3:p.Ile131Val
ENST00000358309.3:c.487A>G	ENSP00000351059.3:p.Ile163Val
ENST00000399220.2:c.391A>G	ENSP00000382166.2:p.Ile131Val
ENST00000435290.1:c.391A>G	ENSP00000394960.1:p.Ile131Val
ENST00000541347.5:c.391A>G	ENSP00000439140.1:p.Ile131Val
ENST00000542107.5:c.391A>G	ENSP00000444928.1:p.Ile131Val
NM_001171171.1:c.391A>G	NP_001164642.1:p.Ile131Val
NM_001171172.1:c.391A>G	NP_001164643.1:p.Ile131Val
NM_001171174.1:c.487A>G	NP_001164645.1:p.Ile163Val
NM_001337.3:c.391A>G	NP_001328.1:p.Ile131Val
NM_001337.4:c.391A>G MANE Select	NP_001328.1:p.Ile131Val
NM_001171171.2:c.391A>G	NP_001164642.1:p.Ile131Val
NM_001171172.2:c.391A>G	NP_001164643.1:p.Ile131Val