Canonical Allele Identifier: CA2256959876
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256061A= , CM000679.2:g.34256061A= GRCh38
NC_000017.10:g.32583080A= , CM000679.1:g.32583080A= GRCh37
NC_000017.9:g.29607193A= NCBI36
NG_012123.1:g.5785A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-161A= ENSP00000462156.1:n.77-161A=
ENST00000624362.2:n.777A=
ENST00000225831.4:c.77-161A= MANE Select ENSP00000225831.4:n.77-161A=
ENST00000580907.5:c.77-161A= ENSP00000462156.1:n.77-161A=
ENST00000624362.1:n.844A=
NM_002982.3:c.77-161A= NP_002973.1:n.77-161A=
NM_002982.4:c.77-161A= MANE Select NP_002973.1:n.77-161A=
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