Canonical Allele Identifier: CA73681688

Linked Data

dbSNP Id: rs2856758
gnomAD v2: 3-46411661-A-G
gnomAD v3: 3-46370170-A-G
gnomAD v4: 3-46370170-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370170A>G , CM000665.2:g.46370170A>G GRCh38
NC_000003.11:g.46411661A>G , CM000665.1:g.46411661A>G GRCh37
NC_000003.10:g.46386665A>G NCBI36
NG_012637.1:g.5029A>G

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-329A>G (CCR5) NP_000570.1:n.-329A>G
NM_001100168.1:c.-94A>G (CCR5) NP_001093638.1:n.-94A>G
NR_125406.1:n.565+1074T>C (CCR5AS)
NM_000579.4:c.-329A>G (CCR5) NP_000570.1:n.-329A>G
NM_001100168.2:c.-94A>G (CCR5) NP_001093638.1:n.-94A>G