Canonical Allele Identifier: CA2637210514
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256070-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256070C>G , CM000679.2:g.34256070C>G GRCh38
NC_000017.10:g.32583089C>G , CM000679.1:g.32583089C>G GRCh37
NC_000017.9:g.29607202C>G NCBI36
NG_012123.1:g.5794C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-152C>G ENSP00000462156.1:n.77-152C>G
ENST00000624362.2:n.786C>G
ENST00000225831.4:c.77-152C>G MANE Select ENSP00000225831.4:n.77-152C>G
ENST00000580907.5:c.77-152C>G ENSP00000462156.1:n.77-152C>G
ENST00000624362.1:n.853C>G
NM_002982.3:c.77-152C>G NP_002973.1:n.77-152C>G
NM_002982.4:c.77-152C>G MANE Select NP_002973.1:n.77-152C>G
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