Canonical Allele Identifier: CA499710409
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32583373del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256355del , CM000679.2:g.34256355del GRCh38
NC_000017.10:g.32583374del , CM000679.1:g.32583374del GRCh37
NC_000017.9:g.29607487del NCBI36
NG_012123.1:g.6079del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*12del ENSP00000462156.1:n.*12del
ENST00000624362.2:n.1071del
ENST00000225831.4:c.194+16del MANE Select ENSP00000225831.4:n.194+16del
ENST00000580907.5:c.*12del ENSP00000462156.1:n.*12del
ENST00000582017.1:n.148del
NM_002982.3:c.194+16del NP_002973.1:n.194+16del
NM_002982.4:c.194+16del MANE Select NP_002973.1:n.194+16del