Canonical Allele Identifier: CA2326879

Gene: CX3CR1

Linked Data

• dbSNP Id: rs137947370
• ExAC: 3:39307063 G / A
• gnomAD v2: 3-39307063-G-A
• gnomAD v3: 3-39265572-G-A
• gnomAD v4: 3-39265572-G-A
• MyVariant Identifiers: chr3:g.39307063G>A (hg19) ; chr3:g.39265572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265572G>A , CM000665.2:g.39265572G>A	GRCh38
NC_000003.11:g.39307063G>A , CM000665.1:g.39307063G>A	GRCh37
NC_000003.10:g.39282067G>A	NCBI36
NG_016362.1:g.21164C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.938C>T MANE Select	ENSP00000382166.3:p.Ala313Val
ENST00000358309.3:c.1034C>T	ENSP00000351059.3:p.Ala345Val
ENST00000399220.2:c.938C>T	ENSP00000382166.2:p.Ala313Val
ENST00000541347.5:c.938C>T	ENSP00000439140.1:p.Ala313Val
ENST00000542107.5:c.938C>T	ENSP00000444928.1:p.Ala313Val
NM_001171171.1:c.938C>T	NP_001164642.1:p.Ala313Val
NM_001171172.1:c.938C>T	NP_001164643.1:p.Ala313Val
NM_001171174.1:c.1034C>T	NP_001164645.1:p.Ala345Val
NM_001337.3:c.938C>T	NP_001328.1:p.Ala313Val
NM_001337.4:c.938C>T MANE Select	NP_001328.1:p.Ala313Val
NM_001171171.2:c.938C>T	NP_001164642.1:p.Ala313Val
NM_001171172.2:c.938C>T	NP_001164643.1:p.Ala313Val