Canonical Allele Identifier: CA2256959939
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256206G= , CM000679.2:g.34256206G= GRCh38
NC_000017.10:g.32583225G= , CM000679.1:g.32583225G= GRCh37
NC_000017.9:g.29607338G= NCBI36
NG_012123.1:g.5930G=

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-16G= ENSP00000462156.1:n.77-16G=
ENST00000624362.2:n.922G=
ENST00000225831.4:c.77-16G= MANE Select ENSP00000225831.4:n.77-16G=
ENST00000580907.5:c.77-16G= ENSP00000462156.1:n.77-16G=
ENST00000624362.1:n.989G=
NM_002982.3:c.77-16G= NP_002973.1:n.77-16G=
NM_002982.4:c.77-16G= MANE Select NP_002973.1:n.77-16G=
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