Canonical Allele Identifier: CA2256959852
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1907674011
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34255993C>T , CM000679.2:g.34255993C>T GRCh38
NC_000017.10:g.32583012C>T , CM000679.1:g.32583012C>T GRCh37
NC_000017.9:g.29607125C>T NCBI36
NG_012123.1:g.5717C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.77-229C>T ENSP00000462156.1:n.77-229C>T
ENST00000624362.2:n.709C>T
ENST00000225831.4:c.77-229C>T MANE Select ENSP00000225831.4:n.77-229C>T
ENST00000580907.5:c.77-229C>T ENSP00000462156.1:n.77-229C>T
ENST00000624362.1:n.776C>T
NM_002982.3:c.77-229C>T NP_002973.1:n.77-229C>T
NM_002982.4:c.77-229C>T MANE Select NP_002973.1:n.77-229C>T
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