Canonical Allele Identifier: CA542616769

Gene: CX3CR1

Linked Data

• dbSNP Id: rs1349949312
• gnomAD v2: 3-39306780-C-T
• gnomAD v3: 3-39265289-C-T
• gnomAD v4: 3-39265289-C-T
• MyVariant Identifiers: chr3:g.39306780C>T (hg19) ; chr3:g.39265289C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265289C>T , CM000665.2:g.39265289C>T	GRCh38
NC_000003.11:g.39306780C>T , CM000665.1:g.39306780C>T	GRCh37
NC_000003.10:g.39281784C>T	NCBI36
NG_016362.1:g.21447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.*153G>A MANE Select	ENSP00000382166.3:n.*153G>A
ENST00000358309.3:c.*153G>A	ENSP00000351059.3:n.*153G>A
ENST00000399220.2:c.*153G>A	ENSP00000382166.2:n.*153G>A
ENST00000541347.5:c.*153G>A	ENSP00000439140.1:n.*153G>A
ENST00000542107.5:c.*153G>A	ENSP00000444928.1:n.*153G>A
NM_001171171.1:c.*153G>A	NP_001164642.1:n.*153G>A
NM_001171172.1:c.*153G>A	NP_001164643.1:n.*153G>A
NM_001171174.1:c.*153G>A	NP_001164645.1:n.*153G>A
NM_001337.3:c.*153G>A	NP_001328.1:n.*153G>A
NM_001337.4:c.*153G>A MANE Select	NP_001328.1:n.*153G>A
NM_001171171.2:c.*153G>A	NP_001164642.1:n.*153G>A
NM_001171172.2:c.*153G>A	NP_001164643.1:n.*153G>A