Canonical Allele Identifier: CA2577557224
Gene: CX3CR1 HGNC NCBI

Linked Data

gnomAD v4: 3-39265364-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265364C>T , CM000665.2:g.39265364C>T GRCh38
NC_000003.11:g.39306855C>T , CM000665.1:g.39306855C>T GRCh37
NC_000003.10:g.39281859C>T NCBI36
NG_016362.1:g.21372G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.*78G>A MANE Select ENSP00000382166.3:n.*78G>A
ENST00000358309.3:c.*78G>A ENSP00000351059.3:n.*78G>A
ENST00000399220.2:c.*78G>A ENSP00000382166.2:n.*78G>A
ENST00000541347.5:c.*78G>A ENSP00000439140.1:n.*78G>A
ENST00000542107.5:c.*78G>A ENSP00000444928.1:n.*78G>A
NM_001171171.1:c.*78G>A NP_001164642.1:n.*78G>A
NM_001171172.1:c.*78G>A NP_001164643.1:n.*78G>A
NM_001171174.1:c.*78G>A NP_001164645.1:n.*78G>A
NM_001337.3:c.*78G>A NP_001328.1:n.*78G>A
NM_001337.4:c.*78G>A MANE Select NP_001328.1:n.*78G>A
NM_001171171.2:c.*78G>A NP_001164642.1:n.*78G>A
NM_001171172.2:c.*78G>A NP_001164643.1:n.*78G>A