Canonical Allele Identifier: CA2354760
Gene: CCR5 HGNC NCBI
CCR5AS HGNC NCBI

Linked Data

dbSNP Id: rs768291615
ExAC: 3:46415376 A / G
gnomAD v2: 3-46415376-A-G
gnomAD v3: 3-46373885-A-G
gnomAD v4: 3-46373885-A-G
MyVariant Identifiers: chr3:g.46415376A>G (hg19) chr3:g.46373885A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373885A>G , CM000665.2:g.46373885A>G GRCh38
NC_000003.11:g.46415376A>G , CM000665.1:g.46415376A>G GRCh37
NC_000003.10:g.46390380A>G NCBI36
NG_012637.1:g.8744A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.983A>G (CCR5) MANE Select ENSP00000292303.4:p.Gln328Arg
ENST00000292303.4:c.983A>G (CCR5) ENSP00000292303.4:p.Gln328Arg
ENST00000445772.1:c.983A>G (CCR5) ENSP00000404881.1:p.Gln328Arg
NM_000579.3:c.983A>G (CCR5) NP_000570.1:p.Gln328Arg
NM_001100168.1:c.983A>G (CCR5) NP_001093638.1:p.Gln328Arg
NR_125406.1:n.392-2468T>C (CCR5AS)
NM_000579.4:c.983A>G (CCR5) NP_000570.1:p.Gln328Arg
NM_001100168.2:c.983A>G (CCR5) NP_001093638.1:p.Gln328Arg
NM_001394783.1:c.983A>G (CCR5) MANE Select NP_001381712.1:p.Gln328Arg
Search 100 bp 5'
Search 100 bp 3'