Canonical Allele Identifier: CA2637210028
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34255429-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255429A>G , CM000679.2:g.34255429A>G GRCh38
NC_000017.10:g.32582448A>G , CM000679.1:g.32582448A>G GRCh37
NC_000017.9:g.29606561A>G NCBI36
NG_012123.1:g.5153A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.76+4A>G ENSP00000462156.1:n.76+4A>G
ENST00000624362.2:n.145A>G
ENST00000225831.4:c.76+4A>G MANE Select ENSP00000225831.4:n.76+4A>G
ENST00000580907.5:c.76+4A>G ENSP00000462156.1:n.76+4A>G
ENST00000624362.1:n.212A>G
NM_002982.3:c.76+4A>G NP_002973.1:n.76+4A>G
NM_002982.4:c.76+4A>G MANE Select NP_002973.1:n.76+4A>G
Search 100 bp 5'
Search 100 bp 3'