Canonical Allele Identifier: CA499710303
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32582410A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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