Canonical Allele Identifier: CA290054786
Gene: CCL5 HGNC NCBI

Linked Data

dbSNP Id: rs1045722277
MyVariant Identifiers: chr17:g.35880711T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880711T>C , CM000679.2:g.35880711T>C GRCh38
NC_000017.9:g.31231828T>C NCBI36
NG_015990.1:g.4663A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000605509.2:c.-18+18A>G ENSP00000474141.2:n.-18+18A>G
ENST00000605140.5:c.-18+18A>G ENSP00000475057.1:n.-18+18A>G
XR_934696.1:n.197-3671T>C
XR_934697.1:n.200-3671T>C
XR_001752852.1:n.426+637T>C
XR_934696.2:n.91-3671T>C
XR_934697.2:n.91-3671T>C