Canonical Allele Identifier: CA2665159084
Gene: CX3CR1 HGNC NCBI

Linked Data

gnomAD v4: 3-39265350-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265350G>T , CM000665.2:g.39265350G>T GRCh38
NC_000003.11:g.39306841G>T , CM000665.1:g.39306841G>T GRCh37
NC_000003.10:g.39281845G>T NCBI36
NG_016362.1:g.21386C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.*92C>A MANE Select ENSP00000382166.3:n.*92C>A
ENST00000358309.3:c.*92C>A ENSP00000351059.3:n.*92C>A
ENST00000399220.2:c.*92C>A ENSP00000382166.2:n.*92C>A
ENST00000541347.5:c.*92C>A ENSP00000439140.1:n.*92C>A
ENST00000542107.5:c.*92C>A ENSP00000444928.1:n.*92C>A
NM_001171171.1:c.*92C>A NP_001164642.1:n.*92C>A
NM_001171172.1:c.*92C>A NP_001164643.1:n.*92C>A
NM_001171174.1:c.*92C>A NP_001164645.1:n.*92C>A
NM_001337.3:c.*92C>A NP_001328.1:n.*92C>A
NM_001337.4:c.*92C>A MANE Select NP_001328.1:n.*92C>A
NM_001171171.2:c.*92C>A NP_001164642.1:n.*92C>A
NM_001171172.2:c.*92C>A NP_001164643.1:n.*92C>A