Canonical Allele Identifier: CA906954210

Gene: CX3CR1

Linked Data

• dbSNP Id: rs1365057207
• gnomAD v3: 3-39279706-C-A
• gnomAD v4: 3-39279706-C-A
• MyVariant Identifiers: chr3:g.39321197C>A (hg19) ; chr3:g.39279706C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.39279706C>A , CM000665.2:g.39279706C>A	GRCh38
NC_000003.11:g.39321197C>A , CM000665.1:g.39321197C>A	GRCh37
NC_000003.10:g.39296201C>A	NCBI36
NG_016362.1:g.7030G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399220.3:c.-10+248G>T MANE Select	ENSP00000382166.3:n.-10+248G>T
ENST00000358309.3:c.87+1903G>T	ENSP00000351059.3:n.87+1903G>T
ENST00000399220.2:c.-10+248G>T	ENSP00000382166.2:n.-10+248G>T
ENST00000412814.1:c.-10+1337G>T	ENSP00000408835.1:n.-10+1337G>T
ENST00000435290.1:c.-10+543G>T	ENSP00000394960.1:n.-10+543G>T
ENST00000541347.5:c.-10+1337G>T	ENSP00000439140.1:n.-10+1337G>T
ENST00000542107.5:c.-10+543G>T	ENSP00000444928.1:n.-10+543G>T
NM_001171171.1:c.-10+1337G>T	NP_001164642.1:n.-10+1337G>T
NM_001171172.1:c.-10+543G>T	NP_001164643.1:n.-10+543G>T
NM_001171174.1:c.87+1903G>T	NP_001164645.1:n.87+1903G>T
NM_001337.3:c.-10+248G>T	NP_001328.1:n.-10+248G>T
NM_001337.4:c.-10+248G>T MANE Select	NP_001328.1:n.-10+248G>T
NM_001171171.2:c.-10+1337G>T	NP_001164642.1:n.-10+1337G>T
NM_001171172.2:c.-10+543G>T	NP_001164643.1:n.-10+543G>T