Canonical Allele Identifier: CA289528761
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs886567880
MyVariant Identifiers: chr17:g.32583524C>G (hg19) chr17:g.34256505C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256505C>G , CM000679.2:g.34256505C>G GRCh38
NC_000017.10:g.32583524C>G , CM000679.1:g.32583524C>G GRCh37
NC_000017.9:g.29607637C>G NCBI36
NG_012123.1:g.6229C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*162C>G ENSP00000462156.1:n.*162C>G
ENST00000624362.2:n.1221C>G
ENST00000225831.4:c.194+166C>G MANE Select ENSP00000225831.4:n.194+166C>G
ENST00000580907.5:c.*162C>G ENSP00000462156.1:n.*162C>G
ENST00000582017.1:n.298C>G
NM_002982.3:c.194+166C>G NP_002973.1:n.194+166C>G
NM_002982.4:c.194+166C>G MANE Select NP_002973.1:n.194+166C>G
Search 100 bp 5'
Search 100 bp 3'