Canonical Allele Identifier: CA399060368
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256341T>C , CM000679.2:g.34256341T>C GRCh38
NC_000017.10:g.32583360T>C , CM000679.1:g.32583360T>C GRCh37
NC_000017.9:g.29607473T>C NCBI36
NG_012123.1:g.6065T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.196T>C ENSP00000462156.1:p.Ter66Arg
ENST00000624362.2:n.1057T>C
ENST00000225831.4:c.194+2T>C MANE Select ENSP00000225831.4:n.194+2T>C
ENST00000580907.5:c.196T>C ENSP00000462156.1:p.Ter66Arg
ENST00000582017.1:n.134T>C
NM_002982.3:c.194+2T>C NP_002973.1:n.194+2T>C
NM_002982.4:c.194+2T>C MANE Select NP_002973.1:n.194+2T>C