Canonical Allele Identifier: CA433341803

Gene: CX3CR1

Linked Data

• dbSNP Id: rs2040687549
• COSMIC: COSM280240 ; COSM1537864
• MyVariant Identifiers: chr3:g.39307287G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265796G>A , CM000665.2:g.39265796G>A	GRCh38
NC_000003.11:g.39307287G>A , CM000665.1:g.39307287G>A	GRCh37
NC_000003.10:g.39282291G>A	NCBI36
NG_016362.1:g.20940C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.714C>T MANE Select	ENSP00000382166.3:p.Ile238=
ENST00000358309.3:c.810C>T	ENSP00000351059.3:p.Ile270=
ENST00000399220.2:c.714C>T	ENSP00000382166.2:p.Ile238=
ENST00000541347.5:c.714C>T	ENSP00000439140.1:p.Ile238=
ENST00000542107.5:c.714C>T	ENSP00000444928.1:p.Ile238=
NM_001171171.1:c.714C>T	NP_001164642.1:p.Ile238=
NM_001171172.1:c.714C>T	NP_001164643.1:p.Ile238=
NM_001171174.1:c.810C>T	NP_001164645.1:p.Ile270=
NM_001337.3:c.714C>T	NP_001328.1:p.Ile238=
NM_001337.4:c.714C>T MANE Select	NP_001328.1:p.Ile238=
NM_001171171.2:c.714C>T	NP_001164642.1:p.Ile238=
NM_001171172.2:c.714C>T	NP_001164643.1:p.Ile238=