Canonical Allele Identifier: CA399060268
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256328A>C , CM000679.2:g.34256328A>C GRCh38
NC_000017.10:g.32583347A>C , CM000679.1:g.32583347A>C GRCh37
NC_000017.9:g.29607460A>C NCBI36
NG_012123.1:g.6052A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.183A>C ENSP00000462156.1:p.Lys61Asn
ENST00000624362.2:n.1044A>C
ENST00000225831.4:c.183A>C MANE Select ENSP00000225831.4:p.Lys61Asn
ENST00000580907.5:c.183A>C ENSP00000462156.1:p.Lys61Asn
ENST00000582017.1:n.121A>C
NM_002982.3:c.183A>C NP_002973.1:p.Lys61Asn
NM_002982.4:c.183A>C MANE Select NP_002973.1:p.Lys61Asn