Canonical Allele Identifier: CA2256960039
Gene: CCL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256449A= , CM000679.2:g.34256449A= GRCh38
NC_000017.10:g.32583468A= , CM000679.1:g.32583468A= GRCh37
NC_000017.9:g.29607581A= NCBI36
NG_012123.1:g.6173A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*106A= ENSP00000462156.1:n.*106A=
ENST00000624362.2:n.1165A=
ENST00000225831.4:c.194+110A= MANE Select ENSP00000225831.4:n.194+110A=
ENST00000580907.5:c.*106A= ENSP00000462156.1:n.*106A=
ENST00000582017.1:n.242A=
NM_002982.3:c.194+110A= NP_002973.1:n.194+110A=
NM_002982.4:c.194+110A= MANE Select NP_002973.1:n.194+110A=
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