Canonical Allele Identifier: CA2576229868
Gene: CCL8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320726C>T , CM000679.2:g.34320726C>T GRCh38
NC_000017.10:g.32647745C>T , CM000679.1:g.32647745C>T GRCh37
NC_000017.9:g.29671858C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-76C>T MANE Select ENSP00000378118.1:n.195-76C>T
ENST00000394620.1:c.195-76C>T ENSP00000378118.1:n.195-76C>T
NM_005623.2:c.195-76C>T NP_005614.2:n.195-76C>T
NM_005623.3:c.195-76C>T MANE Select NP_005614.2:n.195-76C>T