Canonical Allele Identifier: CA1047499389

Linked Data

gnomAD v3: 3-46370387-C-A
gnomAD v4: 3-46370387-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370387C>A , CM000665.2:g.46370387C>A GRCh38
NC_000003.11:g.46411878C>A , CM000665.1:g.46411878C>A GRCh37
NC_000003.10:g.46386882C>A NCBI36
NG_012637.1:g.5246C>A

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+189C>A (CCR5) NP_000570.1:n.-301+189C>A
NM_001100168.1:c.-66+189C>A (CCR5) NP_001093638.1:n.-66+189C>A
NR_125406.1:n.565+857G>T (CCR5AS)
NM_000579.4:c.-301+189C>A (CCR5) NP_000570.1:n.-301+189C>A
NM_001100168.2:c.-66+189C>A (CCR5) NP_001093638.1:n.-66+189C>A