Canonical Allele Identifier: CA2637210789
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256512-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256515del , CM000679.2:g.34256515del GRCh38
NC_000017.10:g.32583534del , CM000679.1:g.32583534del GRCh37
NC_000017.9:g.29607647del NCBI36
NG_012123.1:g.6239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*172del ENSP00000462156.1:n.*172del
ENST00000624362.2:n.1231del
ENST00000225831.4:c.194+176del MANE Select ENSP00000225831.4:n.194+176del
ENST00000580907.5:c.*172del ENSP00000462156.1:n.*172del
ENST00000582017.1:n.308del
NM_002982.3:c.194+176del NP_002973.1:n.194+176del
NM_002982.4:c.194+176del MANE Select NP_002973.1:n.194+176del
Search 100 bp 5'
Search 100 bp 3'