Canonical Allele Identifier: CA499710301

Gene: CCL2

Linked Data

• MyVariant Identifiers: chr17:g.32582410A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.34255391A>T , CM000679.2:g.34255391A>T	GRCh38
NC_000017.10:g.32582410A>T , CM000679.1:g.32582410A>T	GRCh37
NC_000017.9:g.29606523A>T	NCBI36
NG_012123.1:g.5115A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580907.6:c.42A>T	ENSP00000462156.1:p.Ala14=
ENST00000624362.2:n.107A>T
ENST00000225831.4:c.42A>T MANE Select	ENSP00000225831.4:p.Ala14=
ENST00000580907.5:c.42A>T	ENSP00000462156.1:p.Ala14=
ENST00000624362.1:n.174A>T
NM_002982.3:c.42A>T	NP_002973.1:p.Ala14=
NM_002982.4:c.42A>T MANE Select	NP_002973.1:p.Ala14=