Canonical Allele Identifier: CA2256960021
Gene: CCL2 HGNC NCBI

Linked Data

dbSNP Id: rs1567641003
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256406T>C , CM000679.2:g.34256406T>C GRCh38
NC_000017.10:g.32583425T>C , CM000679.1:g.32583425T>C GRCh37
NC_000017.9:g.29607538T>C NCBI36
NG_012123.1:g.6130T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000580907.6:c.*63T>C ENSP00000462156.1:n.*63T>C
ENST00000624362.2:n.1122T>C
ENST00000225831.4:c.194+67T>C MANE Select ENSP00000225831.4:n.194+67T>C
ENST00000580907.5:c.*63T>C ENSP00000462156.1:n.*63T>C
ENST00000582017.1:n.199T>C
NM_002982.3:c.194+67T>C NP_002973.1:n.194+67T>C
NM_002982.4:c.194+67T>C MANE Select NP_002973.1:n.194+67T>C
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