Canonical Allele Identifier: CA8495413
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs771009864
ExAC: 17:32582455 C / T
gnomAD v2: 17-32582455-C-T
gnomAD v3: 17-34255436-C-T
gnomAD v4: 17-34255436-C-T
MyVariant Identifiers: chr17:g.32582455C>T (hg19) chr17:g.32582455_32582458delinsTTCT (hg19) chr17:g.34255436C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255436C>T , CM000679.2:g.34255436C>T GRCh38
NC_000017.10:g.32582455C>T , CM000679.1:g.32582455C>T GRCh37
NC_000017.9:g.29606568C>T NCBI36
NG_012123.1:g.5160C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.76+11C>T ENSP00000462156.1:n.76+11C>T
ENST00000624362.2:n.152C>T
ENST00000225831.4:c.76+11C>T MANE Select ENSP00000225831.4:n.76+11C>T
ENST00000580907.5:c.76+11C>T ENSP00000462156.1:n.76+11C>T
ENST00000624362.1:n.219C>T
NM_002982.3:c.76+11C>T NP_002973.1:n.76+11C>T
NM_002982.4:c.76+11C>T MANE Select NP_002973.1:n.76+11C>T
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