Canonical Allele Identifier: CA8495431
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs752116674
ExAC: 17:32583216 T / C
gnomAD v2: 17-32583216-T-C
gnomAD v4: 17-34256197-T-C
MyVariant Identifiers: chr17:g.32583216T>C (hg19) chr17:g.34256197T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256197T>C , CM000679.2:g.34256197T>C GRCh38
NC_000017.10:g.32583216T>C , CM000679.1:g.32583216T>C GRCh37
NC_000017.9:g.29607329T>C NCBI36
NG_012123.1:g.5921T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-25T>C ENSP00000462156.1:n.77-25T>C
ENST00000624362.2:n.913T>C
ENST00000225831.4:c.77-25T>C MANE Select ENSP00000225831.4:n.77-25T>C
ENST00000580907.5:c.77-25T>C ENSP00000462156.1:n.77-25T>C
ENST00000624362.1:n.980T>C
NM_002982.3:c.77-25T>C NP_002973.1:n.77-25T>C
NM_002982.4:c.77-25T>C MANE Select NP_002973.1:n.77-25T>C
Search 100 bp 5'
Search 100 bp 3'