Canonical Allele Identifier: CA399060060
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32583292T>G (hg19) chr17:g.34256273T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256273T>G , CM000679.2:g.34256273T>G GRCh38
NC_000017.10:g.32583292T>G , CM000679.1:g.32583292T>G GRCh37
NC_000017.9:g.29607405T>G NCBI36
NG_012123.1:g.5997T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.128T>G ENSP00000462156.1:p.Ile43Ser
ENST00000624362.2:n.989T>G
ENST00000225831.4:c.128T>G MANE Select ENSP00000225831.4:p.Ile43Ser
ENST00000580907.5:c.128T>G ENSP00000462156.1:p.Ile43Ser
ENST00000582017.1:n.66T>G
NM_002982.3:c.128T>G NP_002973.1:p.Ile43Ser
NM_002982.4:c.128T>G MANE Select NP_002973.1:p.Ile43Ser
Search 100 bp 5'
Search 100 bp 3'