Canonical Allele Identifier: CA399059814

Gene: CCL2

Linked Data

• gnomAD v4: 17-34255423-C-T
• MyVariant Identifiers: chr17:g.32582442C>T (hg19) ; chr17:g.34255423C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.34255423C>T , CM000679.2:g.34255423C>T	GRCh38
NC_000017.10:g.32582442C>T , CM000679.1:g.32582442C>T	GRCh37
NC_000017.9:g.29606555C>T	NCBI36
NG_012123.1:g.5147C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580907.6:c.74C>T	ENSP00000462156.1:p.Pro25Leu
ENST00000624362.2:n.139C>T
ENST00000225831.4:c.74C>T MANE Select	ENSP00000225831.4:p.Pro25Leu
ENST00000580907.5:c.74C>T	ENSP00000462156.1:p.Pro25Leu
ENST00000624362.1:n.206C>T
NM_002982.3:c.74C>T	NP_002973.1:p.Pro25Leu
NM_002982.4:c.74C>T MANE Select	NP_002973.1:p.Pro25Leu