Canonical Allele Identifier: CA2256960042
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs536707537
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256451G>A , CM000679.2:g.34256451G>A GRCh38
NC_000017.10:g.32583470G>A , CM000679.1:g.32583470G>A GRCh37
NC_000017.9:g.29607583G>A NCBI36
NG_012123.1:g.6175G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*108G>A ENSP00000462156.1:n.*108G>A
ENST00000624362.2:n.1167G>A
ENST00000225831.4:c.194+112G>A MANE Select ENSP00000225831.4:n.194+112G>A
ENST00000580907.5:c.*108G>A ENSP00000462156.1:n.*108G>A
ENST00000582017.1:n.244G>A
NM_002982.3:c.194+112G>A NP_002973.1:n.194+112G>A
NM_002982.4:c.194+112G>A MANE Select NP_002973.1:n.194+112G>A
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