Canonical Allele Identifier: CA433341731
Gene: CX3CR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.39307167A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265676A>T , CM000665.2:g.39265676A>T GRCh38
NC_000003.11:g.39307167A>T , CM000665.1:g.39307167A>T GRCh37
NC_000003.10:g.39282171A>T NCBI36
NG_016362.1:g.21060T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399220.3:c.834T>A MANE Select ENSP00000382166.3:p.Thr278=
ENST00000358309.3:c.930T>A ENSP00000351059.3:p.Thr310=
ENST00000399220.2:c.834T>A ENSP00000382166.2:p.Thr278=
ENST00000541347.5:c.834T>A ENSP00000439140.1:p.Thr278=
ENST00000542107.5:c.834T>A ENSP00000444928.1:p.Thr278=
NM_001171171.1:c.834T>A NP_001164642.1:p.Thr278=
NM_001171172.1:c.834T>A NP_001164643.1:p.Thr278=
NM_001171174.1:c.930T>A NP_001164645.1:p.Thr310=
NM_001337.3:c.834T>A NP_001328.1:p.Thr278=
NM_001337.4:c.834T>A MANE Select NP_001328.1:p.Thr278=
NM_001171171.2:c.834T>A NP_001164642.1:p.Thr278=
NM_001171172.2:c.834T>A NP_001164643.1:p.Thr278=