Canonical Allele Identifier: CA2637213921
Gene: CCL8 HGNC NCBI

Linked Data

gnomAD v4: 17-34320723-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.34320723G>T , CM000679.2:g.34320723G>T GRCh38
NC_000017.10:g.32647742G>T , CM000679.1:g.32647742G>T GRCh37
NC_000017.9:g.29671855G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394620.2:c.195-79G>T MANE Select ENSP00000378118.1:n.195-79G>T
ENST00000394620.1:c.195-79G>T ENSP00000378118.1:n.195-79G>T
NM_005623.2:c.195-79G>T NP_005614.2:n.195-79G>T
NM_005623.3:c.195-79G>T MANE Select NP_005614.2:n.195-79G>T
Search 100 bp 5'
Search 100 bp 3'