Canonical Allele Identifier: CA1358882683

Gene: CX3CR1

Linked Data

• dbSNP Id: rs2040680175
• gnomAD v4: 3-39265323-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265323G>A , CM000665.2:g.39265323G>A	GRCh38
NC_000003.11:g.39306814G>A , CM000665.1:g.39306814G>A	GRCh37
NC_000003.10:g.39281818G>A	NCBI36
NG_016362.1:g.21413C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.*119C>T MANE Select	ENSP00000382166.3:n.*119C>T
ENST00000358309.3:c.*119C>T	ENSP00000351059.3:n.*119C>T
ENST00000399220.2:c.*119C>T	ENSP00000382166.2:n.*119C>T
ENST00000541347.5:c.*119C>T	ENSP00000439140.1:n.*119C>T
ENST00000542107.5:c.*119C>T	ENSP00000444928.1:n.*119C>T
NM_001171171.1:c.*119C>T	NP_001164642.1:n.*119C>T
NM_001171172.1:c.*119C>T	NP_001164643.1:n.*119C>T
NM_001171174.1:c.*119C>T	NP_001164645.1:n.*119C>T
NM_001337.3:c.*119C>T	NP_001328.1:n.*119C>T
NM_001337.4:c.*119C>T MANE Select	NP_001328.1:n.*119C>T
NM_001171171.2:c.*119C>T	NP_001164642.1:n.*119C>T
NM_001171172.2:c.*119C>T	NP_001164643.1:n.*119C>T