Canonical Allele Identifier: CA728286435
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1430085574

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256534C>T , CM000679.2:g.34256534C>T GRCh38
NC_000017.10:g.32583553C>T , CM000679.1:g.32583553C>T GRCh37
NC_000017.9:g.29607666C>T NCBI36
NG_012123.1:g.6258C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*191C>T ENSP00000462156.1:n.*191C>T
ENST00000624362.2:n.1250C>T
ENST00000225831.4:c.195-188C>T MANE Select ENSP00000225831.4:n.195-188C>T
ENST00000580907.5:c.*191C>T ENSP00000462156.1:n.*191C>T
ENST00000582017.1:n.327C>T
NM_002982.3:c.195-188C>T NP_002973.1:n.195-188C>T
NM_002982.4:c.195-188C>T MANE Select NP_002973.1:n.195-188C>T