Canonical Allele Identifier: CA2256959928
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256186T= , CM000679.2:g.34256186T= GRCh38
NC_000017.10:g.32583205T= , CM000679.1:g.32583205T= GRCh37
NC_000017.9:g.29607318T= NCBI36
NG_012123.1:g.5910T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-36T= ENSP00000462156.1:n.77-36T=
ENST00000624362.2:n.902T=
ENST00000225831.4:c.77-36T= MANE Select ENSP00000225831.4:n.77-36T=
ENST00000580907.5:c.77-36T= ENSP00000462156.1:n.77-36T=
ENST00000624362.1:n.969T=
NM_002982.3:c.77-36T= NP_002973.1:n.77-36T=
NM_002982.4:c.77-36T= MANE Select NP_002973.1:n.77-36T=