Canonical Allele Identifier: CA2637210728
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256446-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256446C>A , CM000679.2:g.34256446C>A GRCh38
NC_000017.10:g.32583465C>A , CM000679.1:g.32583465C>A GRCh37
NC_000017.9:g.29607578C>A NCBI36
NG_012123.1:g.6170C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*103C>A ENSP00000462156.1:n.*103C>A
ENST00000624362.2:n.1162C>A
ENST00000225831.4:c.194+107C>A MANE Select ENSP00000225831.4:n.194+107C>A
ENST00000580907.5:c.*103C>A ENSP00000462156.1:n.*103C>A
ENST00000582017.1:n.239C>A
NM_002982.3:c.194+107C>A NP_002973.1:n.194+107C>A
NM_002982.4:c.194+107C>A MANE Select NP_002973.1:n.194+107C>A
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