Canonical Allele Identifier: CA1047048563

Gene: CX3CR1

Linked Data

• dbSNP Id: rs2040679361
• gnomAD v3: 3-39265274-T-C
• gnomAD v4: 3-39265274-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265274T>C , CM000665.2:g.39265274T>C	GRCh38
NC_000003.11:g.39306765T>C , CM000665.1:g.39306765T>C	GRCh37
NC_000003.10:g.39281769T>C	NCBI36
NG_016362.1:g.21462A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.*168A>G MANE Select	ENSP00000382166.3:n.*168A>G
ENST00000358309.3:c.*168A>G	ENSP00000351059.3:n.*168A>G
ENST00000399220.2:c.*168A>G	ENSP00000382166.2:n.*168A>G
ENST00000541347.5:c.*168A>G	ENSP00000439140.1:n.*168A>G
ENST00000542107.5:c.*168A>G	ENSP00000444928.1:n.*168A>G
NM_001171171.1:c.*168A>G	NP_001164642.1:n.*168A>G
NM_001171172.1:c.*168A>G	NP_001164643.1:n.*168A>G
NM_001171174.1:c.*168A>G	NP_001164645.1:n.*168A>G
NM_001337.3:c.*168A>G	NP_001328.1:n.*168A>G
NM_001337.4:c.*168A>G MANE Select	NP_001328.1:n.*168A>G
NM_001171171.2:c.*168A>G	NP_001164642.1:n.*168A>G
NM_001171172.2:c.*168A>G	NP_001164643.1:n.*168A>G