Canonical Allele Identifier: CA2702419956
Gene: CX3CR1 HGNC NCBI

Linked Data

dbSNP Id: rs2125548988

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265358T>C , CM000665.2:g.39265358T>C GRCh38
NC_000003.11:g.39306849T>C , CM000665.1:g.39306849T>C GRCh37
NC_000003.10:g.39281853T>C NCBI36
NG_016362.1:g.21378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.*84A>G MANE Select ENSP00000382166.3:n.*84A>G
ENST00000358309.3:c.*84A>G ENSP00000351059.3:n.*84A>G
ENST00000399220.2:c.*84A>G ENSP00000382166.2:n.*84A>G
ENST00000541347.5:c.*84A>G ENSP00000439140.1:n.*84A>G
ENST00000542107.5:c.*84A>G ENSP00000444928.1:n.*84A>G
NM_001171171.1:c.*84A>G NP_001164642.1:n.*84A>G
NM_001171172.1:c.*84A>G NP_001164643.1:n.*84A>G
NM_001171174.1:c.*84A>G NP_001164645.1:n.*84A>G
NM_001337.3:c.*84A>G NP_001328.1:n.*84A>G
NM_001337.4:c.*84A>G MANE Select NP_001328.1:n.*84A>G
NM_001171171.2:c.*84A>G NP_001164642.1:n.*84A>G
NM_001171172.2:c.*84A>G NP_001164643.1:n.*84A>G