Canonical Allele Identifier: CA2256959570
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255428A= , CM000679.2:g.34255428A= GRCh38
NC_000017.10:g.32582447A= , CM000679.1:g.32582447A= GRCh37
NC_000017.9:g.29606560A= NCBI36
NG_012123.1:g.5152A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.76+3A= ENSP00000462156.1:n.76+3A=
ENST00000624362.2:n.144A=
ENST00000225831.4:c.76+3A= MANE Select ENSP00000225831.4:n.76+3A=
ENST00000580907.5:c.76+3A= ENSP00000462156.1:n.76+3A=
ENST00000624362.1:n.211A=
NM_002982.3:c.76+3A= NP_002973.1:n.76+3A=
NM_002982.4:c.76+3A= MANE Select NP_002973.1:n.76+3A=
Search 100 bp 5'
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