Canonical Allele Identifier: CA2256960025
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs750326048
gnomAD v3: 17-34256411-C-G
gnomAD v4: 17-34256411-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256411C>G , CM000679.2:g.34256411C>G GRCh38
NC_000017.10:g.32583430C>G , CM000679.1:g.32583430C>G GRCh37
NC_000017.9:g.29607543C>G NCBI36
NG_012123.1:g.6135C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*68C>G ENSP00000462156.1:n.*68C>G
ENST00000624362.2:n.1127C>G
ENST00000225831.4:c.194+72C>G MANE Select ENSP00000225831.4:n.194+72C>G
ENST00000580907.5:c.*68C>G ENSP00000462156.1:n.*68C>G
ENST00000582017.1:n.204C>G
NM_002982.3:c.194+72C>G NP_002973.1:n.194+72C>G
NM_002982.4:c.194+72C>G MANE Select NP_002973.1:n.194+72C>G
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