Canonical Allele Identifier: CA8495392
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs773321785
ExAC: 17:32582348 G / T
gnomAD v2: 17-32582348-G-T
gnomAD v4: 17-34255329-G-T
MyVariant Identifiers: chr17:g.32582348G>T (hg19) chr17:g.34255329G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255329G>T , CM000679.2:g.34255329G>T GRCh38
NC_000017.10:g.32582348G>T , CM000679.1:g.32582348G>T GRCh37
NC_000017.9:g.29606461G>T NCBI36
NG_012123.1:g.5053G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.-21G>T ENSP00000462156.1:n.-21G>T
ENST00000624362.2:n.45G>T
ENST00000225831.4:c.-21G>T MANE Select ENSP00000225831.4:n.-21G>T
ENST00000580907.5:c.-21G>T ENSP00000462156.1:n.-21G>T
ENST00000624362.1:n.112G>T
NM_002982.3:c.-21G>T NP_002973.1:n.-21G>T
NM_002982.4:c.-21G>T MANE Select NP_002973.1:n.-21G>T
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