Canonical Allele Identifier: CA399220246

Gene: CCL5

Linked Data

• dbSNP Id: rs1274661249
• gnomAD v4: 17-35880230-A-T
• MyVariant Identifiers: chr17:g.35880230A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880230A>T , CM000679.2:g.35880230A>T	GRCh38
NC_000017.9:g.31231347A>T	NCBI36
NG_015990.1:g.5144T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000603197.6:c.76T>A	ENSP00000474412.1:p.Tyr26Asn
ENST00000605140.6:c.76T>A MANE Select	ENSP00000475057.1:p.Tyr26Asn
ENST00000605509.2:c.76T>A	ENSP00000474141.2:p.Tyr26Asn
ENST00000651122.1:c.76T>A	ENSP00000499138.1:p.Tyr26Asn
ENST00000603197.5:c.76T>A	ENSP00000474412.1:p.Tyr26Asn
ENST00000605140.5:c.76T>A	ENSP00000475057.1:p.Tyr26Asn
ENST00000605509.1:c.62T>A
NM_001278736.1:c.76T>A	NP_001265665.1:p.Tyr26Asn
NM_002985.2:c.76T>A	NP_002976.2:p.Tyr26Asn
XR_934696.1:n.197-4152A>T
XR_934697.1:n.200-4152A>T
XR_001752852.1:n.426+156A>T
XR_934696.2:n.91-4152A>T
XR_934697.2:n.91-4152A>T
NM_001278736.2:c.76T>A	NP_001265665.1:p.Tyr26Asn
NM_002985.3:c.76T>A MANE Select	NP_002976.2:p.Tyr26Asn