Canonical Allele Identifier: CA2637210512
Gene: CCL2 HGNC NCBI

Linked Data

gnomAD v4: 17-34256069-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34256069G>C , CM000679.2:g.34256069G>C GRCh38
NC_000017.10:g.32583088G>C , CM000679.1:g.32583088G>C GRCh37
NC_000017.9:g.29607201G>C NCBI36
NG_012123.1:g.5793G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000580907.6:c.77-153G>C ENSP00000462156.1:n.77-153G>C
ENST00000624362.2:n.785G>C
ENST00000225831.4:c.77-153G>C MANE Select ENSP00000225831.4:n.77-153G>C
ENST00000580907.5:c.77-153G>C ENSP00000462156.1:n.77-153G>C
ENST00000624362.1:n.852G>C
NM_002982.3:c.77-153G>C NP_002973.1:n.77-153G>C
NM_002982.4:c.77-153G>C MANE Select NP_002973.1:n.77-153G>C
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