Canonical Allele Identifier: CA499710302
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34255391-A-G
MyVariant Identifiers: chr17:g.32582410A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255391A>G , CM000679.2:g.34255391A>G GRCh38
NC_000017.10:g.32582410A>G , CM000679.1:g.32582410A>G GRCh37
NC_000017.9:g.29606523A>G NCBI36
NG_012123.1:g.5115A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.42A>G ENSP00000462156.1:p.Ala14=
ENST00000624362.2:n.107A>G
ENST00000225831.4:c.42A>G MANE Select ENSP00000225831.4:p.Ala14=
ENST00000580907.5:c.42A>G ENSP00000462156.1:p.Ala14=
ENST00000624362.1:n.174A>G
NM_002982.3:c.42A>G NP_002973.1:p.Ala14=
NM_002982.4:c.42A>G MANE Select NP_002973.1:p.Ala14=
Search 100 bp 5'
Search 100 bp 3'