Canonical Allele Identifier: CA1047499367

Linked Data

dbSNP Id: rs950835828
gnomAD v3: 3-46370367-C-A
gnomAD v4: 3-46370367-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370367C>A , CM000665.2:g.46370367C>A GRCh38
NC_000003.11:g.46411858C>A , CM000665.1:g.46411858C>A GRCh37
NC_000003.10:g.46386862C>A NCBI36
NG_012637.1:g.5226C>A

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+169C>A (CCR5) NP_000570.1:n.-301+169C>A
NM_001100168.1:c.-66+169C>A (CCR5) NP_001093638.1:n.-66+169C>A
NR_125406.1:n.565+877G>T (CCR5AS)
NM_000579.4:c.-301+169C>A (CCR5) NP_000570.1:n.-301+169C>A
NM_001100168.2:c.-66+169C>A (CCR5) NP_001093638.1:n.-66+169C>A