Canonical Allele Identifier: CA399060023
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs371187910
MyVariant Identifiers: chr17:g.32583284T>A (hg19) chr17:g.34256265T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256265T>A , CM000679.2:g.34256265T>A GRCh38
NC_000017.10:g.32583284T>A , CM000679.1:g.32583284T>A GRCh37
NC_000017.9:g.29607397T>A NCBI36
NG_012123.1:g.5989T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.120T>A ENSP00000462156.1:p.Asn40Lys
ENST00000624362.2:n.981T>A
ENST00000225831.4:c.120T>A MANE Select ENSP00000225831.4:p.Asn40Lys
ENST00000580907.5:c.120T>A ENSP00000462156.1:p.Asn40Lys
ENST00000582017.1:n.58T>A
NM_002982.3:c.120T>A NP_002973.1:p.Asn40Lys
NM_002982.4:c.120T>A MANE Select NP_002973.1:p.Asn40Lys
Search 100 bp 5'
Search 100 bp 3'