Canonical Allele Identifier: CA2354769

Linked Data

dbSNP Id: rs764318467
gnomAD v2: 3-46415394-G-A
gnomAD v3: 3-46373903-G-A
gnomAD v4: 3-46373903-G-A
COSMIC: COSM239215

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373903G>A , CM000665.2:g.46373903G>A GRCh38
NC_000003.11:g.46415394G>A , CM000665.1:g.46415394G>A GRCh37
NC_000003.10:g.46390398G>A NCBI36
NG_012637.1:g.8762G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.1001G>A (CCR5) MANE Select ENSP00000292303.4:p.Arg334Gln
ENST00000292303.4:c.1001G>A (CCR5) ENSP00000292303.4:p.Arg334Gln
ENST00000445772.1:c.1001G>A (CCR5) ENSP00000404881.1:p.Arg334Gln
NM_000579.3:c.1001G>A (CCR5) NP_000570.1:p.Arg334Gln
NM_001100168.1:c.1001G>A (CCR5) NP_001093638.1:p.Arg334Gln
NR_125406.1:n.392-2486C>T (CCR5AS)
NM_000579.4:c.1001G>A (CCR5) NP_000570.1:p.Arg334Gln
NM_001100168.2:c.1001G>A (CCR5) NP_001093638.1:p.Arg334Gln
NM_001394783.1:c.1001G>A (CCR5) MANE Select NP_001381712.1:p.Arg334Gln