Canonical Allele Identifier: CA2256960056
Gene: CCL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256491_34256492delinsAC , CM000679.2:g.34256491_34256492delinsAC GRCh38
NC_000017.10:g.32583510_32583511delinsAC , CM000679.1:g.32583510_32583511delinsAC GRCh37
NC_000017.9:g.29607623_29607624delinsAC NCBI36
NG_012123.1:g.6215_6216delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*148_*149delinsAC ENSP00000462156.1:n.*148_*149delinsAC
ENST00000624362.2:n.1207_1208delinsAC
ENST00000225831.4:c.194+152_194+153delinsAC MANE Select ENSP00000225831.4:n.194+152_194+153delinsAC
ENST00000580907.5:c.*148_*149delinsAC ENSP00000462156.1:n.*148_*149delinsAC
ENST00000582017.1:n.284_285delinsAC
NM_002982.3:c.194+152_194+153delinsAC NP_002973.1:n.194+152_194+153delinsAC
NM_002982.4:c.194+152_194+153delinsAC MANE Select NP_002973.1:n.194+152_194+153delinsAC