Canonical Allele Identifier: CA2637210027
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255429_34255431dup , CM000679.2:g.34255429_34255431dup GRCh38
NC_000017.10:g.32582448_32582450dup , CM000679.1:g.32582448_32582450dup GRCh37
NC_000017.9:g.29606561_29606563dup NCBI36
NG_012123.1:g.5153_5155dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.76+4_76+6dup ENSP00000462156.1:n.76+4_76+6dup
ENST00000624362.2:n.145_147dup
ENST00000225831.4:c.76+4_76+6dup MANE Select ENSP00000225831.4:n.76+4_76+6dup
ENST00000580907.5:c.76+4_76+6dup ENSP00000462156.1:n.76+4_76+6dup
ENST00000624362.1:n.212_214dup
NM_002982.3:c.76+4_76+6dup NP_002973.1:n.76+4_76+6dup
NM_002982.4:c.76+4_76+6dup MANE Select NP_002973.1:n.76+4_76+6dup