Canonical Allele Identifier: CA983184258
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907688393
gnomAD v3: 17-34256441-A-G
gnomAD v4: 17-34256441-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256441A>G , CM000679.2:g.34256441A>G GRCh38
NC_000017.10:g.32583460A>G , CM000679.1:g.32583460A>G GRCh37
NC_000017.9:g.29607573A>G NCBI36
NG_012123.1:g.6165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*98A>G ENSP00000462156.1:n.*98A>G
ENST00000624362.2:n.1157A>G
ENST00000225831.4:c.194+102A>G MANE Select ENSP00000225831.4:n.194+102A>G
ENST00000580907.5:c.*98A>G ENSP00000462156.1:n.*98A>G
ENST00000582017.1:n.234A>G
NM_002982.3:c.194+102A>G NP_002973.1:n.194+102A>G
NM_002982.4:c.194+102A>G MANE Select NP_002973.1:n.194+102A>G
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