Canonical Allele Identifier: CA625524298
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1416000717
gnomAD v2: 17-32583002-TCCTCCTTCTC-T
gnomAD v3: 17-34255983-TCCTCCTTCTC-T
gnomAD v4: 17-34255983-TCCTCCTTCTC-T
MyVariant Identifiers: chr17:g.32583003_32583012del (hg19) chr17:g.34255984_34255993del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255984_34255993del , CM000679.2:g.34255984_34255993del GRCh38
NC_000017.10:g.32583003_32583012del , CM000679.1:g.32583003_32583012del GRCh37
NC_000017.9:g.29607116_29607125del NCBI36
NG_012123.1:g.5708_5717del

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-238_77-229del ENSP00000462156.1:n.77-238_77-229del
ENST00000624362.2:n.700_709del
ENST00000225831.4:c.77-238_77-229del MANE Select ENSP00000225831.4:n.77-238_77-229del
ENST00000580907.5:c.77-238_77-229del ENSP00000462156.1:n.77-238_77-229del
ENST00000624362.1:n.767_776del
NM_002982.3:c.77-238_77-229del NP_002973.1:n.77-238_77-229del
NM_002982.4:c.77-238_77-229del MANE Select NP_002973.1:n.77-238_77-229del
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