Canonical Allele Identifier: CA2637210498
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256056-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256056A>T , CM000679.2:g.34256056A>T GRCh38
NC_000017.10:g.32583075A>T , CM000679.1:g.32583075A>T GRCh37
NC_000017.9:g.29607188A>T NCBI36
NG_012123.1:g.5780A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-166A>T ENSP00000462156.1:n.77-166A>T
ENST00000624362.2:n.772A>T
ENST00000225831.4:c.77-166A>T MANE Select ENSP00000225831.4:n.77-166A>T
ENST00000580907.5:c.77-166A>T ENSP00000462156.1:n.77-166A>T
ENST00000624362.1:n.839A>T
NM_002982.3:c.77-166A>T NP_002973.1:n.77-166A>T
NM_002982.4:c.77-166A>T MANE Select NP_002973.1:n.77-166A>T
Search 100 bp 5'
Search 100 bp 3'