Canonical Allele Identifier: CA290054573

Gene: CCL5

Linked Data

• dbSNP Id: rs760825249
• gnomAD v3: 17-35880243-T-C
• gnomAD v4: 17-35880243-T-C
• MyVariant Identifiers: chr17:g.35880243T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880243T>C , CM000679.2:g.35880243T>C	GRCh38
NC_000017.9:g.31231360T>C	NCBI36
NG_015990.1:g.5131A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603197.6:c.63A>G	ENSP00000474412.1:p.Ala21=
ENST00000605140.6:c.63A>G MANE Select	ENSP00000475057.1:p.Ala21=
ENST00000605509.2:c.63A>G	ENSP00000474141.2:p.Ala21=
ENST00000651122.1:c.63A>G	ENSP00000499138.1:p.Ala21=
ENST00000603197.5:c.63A>G	ENSP00000474412.1:p.Ala21=
ENST00000605140.5:c.63A>G	ENSP00000475057.1:p.Ala21=
ENST00000605509.1:c.49A>G
NM_001278736.1:c.63A>G	NP_001265665.1:p.Ala21=
NM_002985.2:c.63A>G	NP_002976.2:p.Ala21=
XR_934696.1:n.197-4139T>C
XR_934697.1:n.200-4139T>C
XR_001752852.1:n.426+169T>C
XR_934696.2:n.91-4139T>C
XR_934697.2:n.91-4139T>C
NM_001278736.2:c.63A>G	NP_001265665.1:p.Ala21=
NM_002985.3:c.63A>G MANE Select	NP_002976.2:p.Ala21=