Canonical Allele Identifier: CA2665159071
Gene: CX3CR1 HGNC NCBI

Linked Data

gnomAD v4: 3-39265334-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.39265334C>A , CM000665.2:g.39265334C>A GRCh38
NC_000003.11:g.39306825C>A , CM000665.1:g.39306825C>A GRCh37
NC_000003.10:g.39281829C>A NCBI36
NG_016362.1:g.21402G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399220.3:c.*108G>T MANE Select ENSP00000382166.3:n.*108G>T
ENST00000358309.3:c.*108G>T ENSP00000351059.3:n.*108G>T
ENST00000399220.2:c.*108G>T ENSP00000382166.2:n.*108G>T
ENST00000541347.5:c.*108G>T ENSP00000439140.1:n.*108G>T
ENST00000542107.5:c.*108G>T ENSP00000444928.1:n.*108G>T
NM_001171171.1:c.*108G>T NP_001164642.1:n.*108G>T
NM_001171172.1:c.*108G>T NP_001164643.1:n.*108G>T
NM_001171174.1:c.*108G>T NP_001164645.1:n.*108G>T
NM_001337.3:c.*108G>T NP_001328.1:n.*108G>T
NM_001337.4:c.*108G>T MANE Select NP_001328.1:n.*108G>T
NM_001171171.2:c.*108G>T NP_001164642.1:n.*108G>T
NM_001171172.2:c.*108G>T NP_001164643.1:n.*108G>T