Canonical Allele Identifier: CA499710199
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582281C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255262C>T , CM000679.2:g.34255262C>T GRCh38
NC_000017.10:g.32582281C>T , CM000679.1:g.32582281C>T GRCh37
NC_000017.9:g.29606394C>T NCBI36
NG_012123.1:g.4986C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624362.1:n.45C>T