Canonical Allele Identifier: CA2256960065
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256506T= , CM000679.2:g.34256506T= GRCh38
NC_000017.10:g.32583525T= , CM000679.1:g.32583525T= GRCh37
NC_000017.9:g.29607638T= NCBI36
NG_012123.1:g.6230T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*163T= ENSP00000462156.1:n.*163T=
ENST00000624362.2:n.1222T=
ENST00000225831.4:c.194+167T= MANE Select ENSP00000225831.4:n.194+167T=
ENST00000580907.5:c.*163T= ENSP00000462156.1:n.*163T=
ENST00000582017.1:n.299T=
NM_002982.3:c.194+167T= NP_002973.1:n.194+167T=
NM_002982.4:c.194+167T= MANE Select NP_002973.1:n.194+167T=
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