Canonical Allele Identifier: CA14448216
Gene: CCL2 HGNC NCBI
COSMIC:
COSN26727645 (not active)
MyVariant.info:
GRCh38 chr17:g.34256892C>T
GRCh37 chr17:g.32583911C>T
gnomAD v2:
17:32583911 C / T
gnomAD v3:
17:34256892 C / T
gnomAD v4:
chr17-34256892-C-T
Joint Max Group AF 0.60439231 (EAS)
Genomes Max Group AF 0.53819157 (EAS)
Exomes Max Group AF 0.61210034 (EAS)
dbSNP:
13900
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256892C>T , CM000679.2:g.34256892C>T GRCh38
NC_000017.10:g.32583911C>T , CM000679.1:g.32583911C>T GRCh37
NC_000017.9:g.29608024C>T NCBI36
NG_012123.1:g.6616C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*549C>T ENSP00000462156.1:n.*549C>T
ENST00000624362.2:n.1608C>T
ENST00000225831.4:c.*65C>T MANE Select ENSP00000225831.4:n.*65C>T
ENST00000582017.1:n.685C>T
NM_002982.3:c.*65C>T NP_002973.1:n.*65C>T
NM_002982.4:c.*65C>T MANE Select NP_002973.1:n.*65C>T
Search 100 bp 5'
Search 100 bp 3'