Canonical Allele Identifier: CA499710324
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582437T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255418T>G , CM000679.2:g.34255418T>G GRCh38
NC_000017.10:g.32582437T>G , CM000679.1:g.32582437T>G GRCh37
NC_000017.9:g.29606550T>G NCBI36
NG_012123.1:g.5142T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.69T>G ENSP00000462156.1:p.Ala23=
ENST00000624362.2:n.134T>G
ENST00000225831.4:c.69T>G MANE Select ENSP00000225831.4:p.Ala23=
ENST00000580907.5:c.69T>G ENSP00000462156.1:p.Ala23=
ENST00000624362.1:n.201T>G
NM_002982.3:c.69T>G NP_002973.1:p.Ala23=
NM_002982.4:c.69T>G MANE Select NP_002973.1:p.Ala23=
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