Canonical Allele Identifier: CA2256960059
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256494C= , CM000679.2:g.34256494C= GRCh38
NC_000017.10:g.32583513C= , CM000679.1:g.32583513C= GRCh37
NC_000017.9:g.29607626C= NCBI36
NG_012123.1:g.6218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*151C= ENSP00000462156.1:n.*151C=
ENST00000624362.2:n.1210C=
ENST00000225831.4:c.194+155C= MANE Select ENSP00000225831.4:n.194+155C=
ENST00000580907.5:c.*151C= ENSP00000462156.1:n.*151C=
ENST00000582017.1:n.287C=
NM_002982.3:c.194+155C= NP_002973.1:n.194+155C=
NM_002982.4:c.194+155C= MANE Select NP_002973.1:n.194+155C=
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