Canonical Allele Identifier: CA289528735
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs945801490
gnomAD v2: 17-32583461-T-A
gnomAD v3: 17-34256442-T-A
gnomAD v4: 17-34256442-T-A
MyVariant Identifiers: chr17:g.32583461T>A (hg19) chr17:g.34256442T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256442T>A , CM000679.2:g.34256442T>A GRCh38
NC_000017.10:g.32583461T>A , CM000679.1:g.32583461T>A GRCh37
NC_000017.9:g.29607574T>A NCBI36
NG_012123.1:g.6166T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*99T>A ENSP00000462156.1:n.*99T>A
ENST00000624362.2:n.1158T>A
ENST00000225831.4:c.194+103T>A MANE Select ENSP00000225831.4:n.194+103T>A
ENST00000580907.5:c.*99T>A ENSP00000462156.1:n.*99T>A
ENST00000582017.1:n.235T>A
NM_002982.3:c.194+103T>A NP_002973.1:n.194+103T>A
NM_002982.4:c.194+103T>A MANE Select NP_002973.1:n.194+103T>A
Search 100 bp 5'
Search 100 bp 3'