Canonical Allele Identifier: CA399059830
Gene: CCL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256222A>T , CM000679.2:g.34256222A>T GRCh38
NC_000017.10:g.32583241A>T , CM000679.1:g.32583241A>T GRCh37
NC_000017.9:g.29607354A>T NCBI36
NG_012123.1:g.5946A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77A>T ENSP00000462156.1:p.Asp26Val
ENST00000624362.2:n.938A>T
ENST00000225831.4:c.77A>T MANE Select ENSP00000225831.4:p.Asp26Val
ENST00000580907.5:c.77A>T ENSP00000462156.1:p.Asp26Val
ENST00000582017.1:n.15A>T
NM_002982.3:c.77A>T NP_002973.1:p.Asp26Val
NM_002982.4:c.77A>T MANE Select NP_002973.1:p.Asp26Val