Canonical Allele Identifier: CA2256959797
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255899C= , CM000679.2:g.34255899C= GRCh38
NC_000017.10:g.32582918C= , CM000679.1:g.32582918C= GRCh37
NC_000017.9:g.29607031C= NCBI36
NG_012123.1:g.5623C=

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-323C= ENSP00000462156.1:n.77-323C=
ENST00000624362.2:n.615C=
ENST00000225831.4:c.77-323C= MANE Select ENSP00000225831.4:n.77-323C=
ENST00000580907.5:c.77-323C= ENSP00000462156.1:n.77-323C=
ENST00000624362.1:n.682C=
NM_002982.3:c.77-323C= NP_002973.1:n.77-323C=
NM_002982.4:c.77-323C= MANE Select NP_002973.1:n.77-323C=
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