Canonical Allele Identifier: CA1362081217

Linked Data

dbSNP Id: rs1701644651
gnomAD v3: 3-46370315-G-A
gnomAD v4: 3-46370315-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370315G>A , CM000665.2:g.46370315G>A GRCh38
NC_000003.11:g.46411806G>A , CM000665.1:g.46411806G>A GRCh37
NC_000003.10:g.46386810G>A NCBI36
NG_012637.1:g.5174G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000579.3:c.-301+117G>A (CCR5) NP_000570.1:n.-301+117G>A
NM_001100168.1:c.-66+117G>A (CCR5) NP_001093638.1:n.-66+117G>A
NR_125406.1:n.565+929C>T (CCR5AS)
NM_000579.4:c.-301+117G>A (CCR5) NP_000570.1:n.-301+117G>A
NM_001100168.2:c.-66+117G>A (CCR5) NP_001093638.1:n.-66+117G>A