Canonical Allele Identifier: CA14377095
Gene: CCL8 HGNC NCBI

Linked Data

dbSNP Id: rs3138037
gnomAD v2: 17-32647744-T-C
gnomAD v3: 17-34320725-T-C
gnomAD v4: 17-34320725-T-C
MyVariant Identifiers: chr17:g.32647744T>C (hg19) chr17:g.34320725T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320725T>C , CM000679.2:g.34320725T>C GRCh38
NC_000017.10:g.32647744T>C , CM000679.1:g.32647744T>C GRCh37
NC_000017.9:g.29671857T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-77T>C MANE Select ENSP00000378118.1:n.195-77T>C
ENST00000394620.1:c.195-77T>C ENSP00000378118.1:n.195-77T>C
NM_005623.2:c.195-77T>C NP_005614.2:n.195-77T>C
NM_005623.3:c.195-77T>C MANE Select NP_005614.2:n.195-77T>C
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