Canonical Allele Identifier: CA2637310287
Gene: CCL5 HGNC NCBI

Linked Data

gnomAD v4: 17-35880316-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880316G>T , CM000679.2:g.35880316G>T GRCh38
NC_000017.9:g.31231433G>T NCBI36
NG_015990.1:g.5058C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.-11C>A ENSP00000474412.1:n.-11C>A
ENST00000605140.6:c.-11C>A MANE Select ENSP00000475057.1:n.-11C>A
ENST00000605509.2:c.-11C>A ENSP00000474141.2:n.-11C>A
ENST00000651122.1:c.-11C>A ENSP00000499138.1:n.-11C>A
ENST00000603197.5:c.-11C>A ENSP00000474412.1:n.-11C>A
ENST00000605140.5:c.-11C>A ENSP00000475057.1:n.-11C>A
NM_001278736.1:c.-11C>A NP_001265665.1:n.-11C>A
NM_002985.2:c.-11C>A NP_002976.2:n.-11C>A
XR_934696.1:n.197-4066G>T
XR_934697.1:n.200-4066G>T
XR_001752852.1:n.426+242G>T
XR_934696.2:n.91-4066G>T
XR_934697.2:n.91-4066G>T
NM_001278736.2:c.-11C>A NP_001265665.1:n.-11C>A
NM_002985.3:c.-11C>A MANE Select NP_002976.2:n.-11C>A
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