Canonical Allele Identifier: CA399060021
Gene: CCL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.32583283A>T (hg19) chr17:g.34256264A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256264A>T , CM000679.2:g.34256264A>T GRCh38
NC_000017.10:g.32583283A>T , CM000679.1:g.32583283A>T GRCh37
NC_000017.9:g.29607396A>T NCBI36
NG_012123.1:g.5988A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.119A>T ENSP00000462156.1:p.Asn40Ile
ENST00000624362.2:n.980A>T
ENST00000225831.4:c.119A>T MANE Select ENSP00000225831.4:p.Asn40Ile
ENST00000580907.5:c.119A>T ENSP00000462156.1:p.Asn40Ile
ENST00000582017.1:n.57A>T
NM_002982.3:c.119A>T NP_002973.1:p.Asn40Ile
NM_002982.4:c.119A>T MANE Select NP_002973.1:p.Asn40Ile
Search 100 bp 5'
Search 100 bp 3'