Canonical Allele Identifier: CA2256959502
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255285G= , CM000679.2:g.34255285G= GRCh38
NC_000017.10:g.32582304G= , CM000679.1:g.32582304G= GRCh37
NC_000017.9:g.29606417G= NCBI36
NG_012123.1:g.5009G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-65G= ENSP00000462156.1:n.-65G=
ENST00000624362.2:n.1G=
ENST00000225831.4:c.-65G= MANE Select ENSP00000225831.4:n.-65G=
ENST00000580907.5:c.-65G= ENSP00000462156.1:n.-65G=
ENST00000624362.1:n.68G=
NM_002982.3:c.-65G= NP_002973.1:n.-65G=
NM_002982.4:c.-65G= MANE Select NP_002973.1:n.-65G=
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