Canonical Allele Identifier: CA983184036

Gene: CCL2

Linked Data

• dbSNP Id: rs1907670780
• gnomAD v3: 17-34255911-TC-T
• gnomAD v4: 17-34255911-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.34255914del , CM000679.2:g.34255914del	GRCh38
NC_000017.10:g.32582933del , CM000679.1:g.32582933del	GRCh37
NC_000017.9:g.29607046del	NCBI36
NG_012123.1:g.5638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580907.6:c.77-308del	ENSP00000462156.1:n.77-308del
ENST00000624362.2:n.630del
ENST00000225831.4:c.77-308del MANE Select	ENSP00000225831.4:n.77-308del
ENST00000580907.5:c.77-308del	ENSP00000462156.1:n.77-308del
ENST00000624362.1:n.697del
NM_002982.3:c.77-308del	NP_002973.1:n.77-308del
NM_002982.4:c.77-308del MANE Select	NP_002973.1:n.77-308del