Canonical Allele Identifier: CA2256994429
Gene: CCL8 HGNC NCBI

Linked Data

dbSNP Id: rs1597604688
gnomAD v3: 17-34320715-G-C
gnomAD v4: 17-34320715-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320715G>C , CM000679.2:g.34320715G>C GRCh38
NC_000017.10:g.32647734G>C , CM000679.1:g.32647734G>C GRCh37
NC_000017.9:g.29671847G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-87G>C MANE Select ENSP00000378118.1:n.195-87G>C
ENST00000394620.1:c.195-87G>C ENSP00000378118.1:n.195-87G>C
NM_005623.2:c.195-87G>C NP_005614.2:n.195-87G>C
NM_005623.3:c.195-87G>C MANE Select NP_005614.2:n.195-87G>C
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