Canonical Allele Identifier: CA73027446

Gene: CX3CR1

Linked Data

• dbSNP Id: rs979436169
• MyVariant Identifiers: chr3:g.39306803G>A (hg19) ; chr3:g.39265312G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265312G>A , CM000665.2:g.39265312G>A	GRCh38
NC_000003.11:g.39306803G>A , CM000665.1:g.39306803G>A	GRCh37
NC_000003.10:g.39281807G>A	NCBI36
NG_016362.1:g.21424C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.*130C>T MANE Select	ENSP00000382166.3:n.*130C>T
ENST00000358309.3:c.*130C>T	ENSP00000351059.3:n.*130C>T
ENST00000399220.2:c.*130C>T	ENSP00000382166.2:n.*130C>T
ENST00000541347.5:c.*130C>T	ENSP00000439140.1:n.*130C>T
ENST00000542107.5:c.*130C>T	ENSP00000444928.1:n.*130C>T
NM_001171171.1:c.*130C>T	NP_001164642.1:n.*130C>T
NM_001171172.1:c.*130C>T	NP_001164643.1:n.*130C>T
NM_001171174.1:c.*130C>T	NP_001164645.1:n.*130C>T
NM_001337.3:c.*130C>T	NP_001328.1:n.*130C>T
NM_001337.4:c.*130C>T MANE Select	NP_001328.1:n.*130C>T
NM_001171171.2:c.*130C>T	NP_001164642.1:n.*130C>T
NM_001171172.2:c.*130C>T	NP_001164643.1:n.*130C>T