Canonical Allele Identifier: CA2256960048
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907689446

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256471G>A , CM000679.2:g.34256471G>A GRCh38
NC_000017.10:g.32583490G>A , CM000679.1:g.32583490G>A GRCh37
NC_000017.9:g.29607603G>A NCBI36
NG_012123.1:g.6195G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*128G>A ENSP00000462156.1:n.*128G>A
ENST00000624362.2:n.1187G>A
ENST00000225831.4:c.194+132G>A MANE Select ENSP00000225831.4:n.194+132G>A
ENST00000580907.5:c.*128G>A ENSP00000462156.1:n.*128G>A
ENST00000582017.1:n.264G>A
NM_002982.3:c.194+132G>A NP_002973.1:n.194+132G>A
NM_002982.4:c.194+132G>A MANE Select NP_002973.1:n.194+132G>A