Canonical Allele Identifier: CA399060079
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32583295C>G (hg19) chr17:g.34256276C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256276C>G , CM000679.2:g.34256276C>G GRCh38
NC_000017.10:g.32583295C>G , CM000679.1:g.32583295C>G GRCh37
NC_000017.9:g.29607408C>G NCBI36
NG_012123.1:g.6000C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.131C>G ENSP00000462156.1:p.Ser44Ter
ENST00000624362.2:n.992C>G
ENST00000225831.4:c.131C>G MANE Select ENSP00000225831.4:p.Ser44Ter
ENST00000580907.5:c.131C>G ENSP00000462156.1:p.Ser44Ter
ENST00000582017.1:n.69C>G
NM_002982.3:c.131C>G NP_002973.1:p.Ser44Ter
NM_002982.4:c.131C>G MANE Select NP_002973.1:p.Ser44Ter
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