Canonical Allele Identifier: CA2224582465
Gene: CX3CL1 HGNC NCBI

Linked Data

dbSNP Id: rs1902241039

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.57376096A>G , CM000678.2:g.57376096A>G GRCh38
NC_000016.9:g.57410008A>G , CM000678.1:g.57410008A>G GRCh37
NC_000016.8:g.55967509A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000006053.7:c.70+3458A>G MANE Select ENSP00000006053.6:n.70+3458A>G
ENST00000006053.6:c.70+3458A>G ENSP00000006053.6:n.70+3458A>G
ENST00000563383.1:c.70+3458A>G ENSP00000456830.1:n.70+3458A>G
ENST00000564948.1:c.70+3458A>G ENSP00000457996.1:n.70+3458A>G
NM_001304392.1:c.-65+3458A>G NP_001291321.1:n.-65+3458A>G
NM_002996.4:c.70+3458A>G NP_002987.1:n.70+3458A>G
NM_001304392.2:c.-65+3458A>G NP_001291321.1:n.-65+3458A>G
NM_002996.5:c.70+3458A>G NP_002987.1:n.70+3458A>G
NM_002996.6:c.70+3458A>G MANE Select NP_002987.1:n.70+3458A>G
NM_001304392.3:c.-65+3458A>G NP_001291321.1:n.-65+3458A>G