Canonical Allele Identifier: CA2637210496
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256053-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256053C>A , CM000679.2:g.34256053C>A GRCh38
NC_000017.10:g.32583072C>A , CM000679.1:g.32583072C>A GRCh37
NC_000017.9:g.29607185C>A NCBI36
NG_012123.1:g.5777C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-169C>A ENSP00000462156.1:n.77-169C>A
ENST00000624362.2:n.769C>A
ENST00000225831.4:c.77-169C>A MANE Select ENSP00000225831.4:n.77-169C>A
ENST00000580907.5:c.77-169C>A ENSP00000462156.1:n.77-169C>A
ENST00000624362.1:n.836C>A
NM_002982.3:c.77-169C>A NP_002973.1:n.77-169C>A
NM_002982.4:c.77-169C>A MANE Select NP_002973.1:n.77-169C>A
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