Canonical Allele Identifier: CA352201721

Gene: CX3CR1

Linked Data

• gnomAD v4: 3-39265878-T-C
• MyVariant Identifiers: chr3:g.39307369T>C (hg19) ; chr3:g.39265878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39265878T>C , CM000665.2:g.39265878T>C	GRCh38
NC_000003.11:g.39307369T>C , CM000665.1:g.39307369T>C	GRCh37
NC_000003.10:g.39282373T>C	NCBI36
NG_016362.1:g.20858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399220.3:c.632A>G MANE Select	ENSP00000382166.3:p.Tyr211Cys
ENST00000358309.3:c.728A>G	ENSP00000351059.3:p.Tyr243Cys
ENST00000399220.2:c.632A>G	ENSP00000382166.2:p.Tyr211Cys
ENST00000541347.5:c.632A>G	ENSP00000439140.1:p.Tyr211Cys
ENST00000542107.5:c.632A>G	ENSP00000444928.1:p.Tyr211Cys
NM_001171171.1:c.632A>G	NP_001164642.1:p.Tyr211Cys
NM_001171172.1:c.632A>G	NP_001164643.1:p.Tyr211Cys
NM_001171174.1:c.728A>G	NP_001164645.1:p.Tyr243Cys
NM_001337.3:c.632A>G	NP_001328.1:p.Tyr211Cys
NM_001337.4:c.632A>G MANE Select	NP_001328.1:p.Tyr211Cys
NM_001171171.2:c.632A>G	NP_001164642.1:p.Tyr211Cys
NM_001171172.2:c.632A>G	NP_001164643.1:p.Tyr211Cys