Canonical Allele Identifier: CA8495429
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs758795760

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256188C>T , CM000679.2:g.34256188C>T GRCh38
NC_000017.10:g.32583207C>T , CM000679.1:g.32583207C>T GRCh37
NC_000017.9:g.29607320C>T NCBI36
NG_012123.1:g.5912C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-34C>T ENSP00000462156.1:n.77-34C>T
ENST00000624362.2:n.904C>T
ENST00000225831.4:c.77-34C>T MANE Select ENSP00000225831.4:n.77-34C>T
ENST00000580907.5:c.77-34C>T ENSP00000462156.1:n.77-34C>T
ENST00000624362.1:n.971C>T
NM_002982.3:c.77-34C>T NP_002973.1:n.77-34C>T
NM_002982.4:c.77-34C>T MANE Select NP_002973.1:n.77-34C>T