Canonical Allele Identifier: CA433341725
Gene: CX3CR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.39307161C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265670C>G , CM000665.2:g.39265670C>G GRCh38
NC_000003.11:g.39307161C>G , CM000665.1:g.39307161C>G GRCh37
NC_000003.10:g.39282165C>G NCBI36
NG_016362.1:g.21066G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399220.3:c.840G>C MANE Select ENSP00000382166.3:p.Thr280=
ENST00000358309.3:c.936G>C ENSP00000351059.3:p.Thr312=
ENST00000399220.2:c.840G>C ENSP00000382166.2:p.Thr280=
ENST00000541347.5:c.840G>C ENSP00000439140.1:p.Thr280=
ENST00000542107.5:c.840G>C ENSP00000444928.1:p.Thr280=
NM_001171171.1:c.840G>C NP_001164642.1:p.Thr280=
NM_001171172.1:c.840G>C NP_001164643.1:p.Thr280=
NM_001171174.1:c.936G>C NP_001164645.1:p.Thr312=
NM_001337.3:c.840G>C NP_001328.1:p.Thr280=
NM_001337.4:c.840G>C MANE Select NP_001328.1:p.Thr280=
NM_001171171.2:c.840G>C NP_001164642.1:p.Thr280=
NM_001171172.2:c.840G>C NP_001164643.1:p.Thr280=