Canonical Allele Identifier: CA2637213923
Gene: CCL8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320728A>C , CM000679.2:g.34320728A>C GRCh38
NC_000017.10:g.32647747A>C , CM000679.1:g.32647747A>C GRCh37
NC_000017.9:g.29671860A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394620.2:c.195-74A>C MANE Select ENSP00000378118.1:n.195-74A>C
ENST00000394620.1:c.195-74A>C ENSP00000378118.1:n.195-74A>C
NM_005623.2:c.195-74A>C NP_005614.2:n.195-74A>C
NM_005623.3:c.195-74A>C MANE Select NP_005614.2:n.195-74A>C