Canonical Allele Identifier: CA625524310
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1445189789
gnomAD v2: 17-32583221-C-T
gnomAD v4: 17-34256202-C-T
MyVariant Identifiers: chr17:g.32583221C>T (hg19) chr17:g.34256202C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256202C>T , CM000679.2:g.34256202C>T GRCh38
NC_000017.10:g.32583221C>T , CM000679.1:g.32583221C>T GRCh37
NC_000017.9:g.29607334C>T NCBI36
NG_012123.1:g.5926C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-20C>T ENSP00000462156.1:n.77-20C>T
ENST00000624362.2:n.918C>T
ENST00000225831.4:c.77-20C>T MANE Select ENSP00000225831.4:n.77-20C>T
ENST00000580907.5:c.77-20C>T ENSP00000462156.1:n.77-20C>T
ENST00000624362.1:n.985C>T
NM_002982.3:c.77-20C>T NP_002973.1:n.77-20C>T
NM_002982.4:c.77-20C>T MANE Select NP_002973.1:n.77-20C>T
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