Canonical Allele Identifier: CA212890
Gene: CCR5 HGNC NCBI
CCR5AS HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.46370771C>T
GRCh37 chr3:g.46412262C>T
gnomAD v2:
3:46412262 C / T
gnomAD v3:
3:46370771 C / T
gnomAD v4:
chr3-46370771-C-T
Joint Max Group AF 0.20039053 (AFR)
Genomes Max Group AF 0.20039053 (AFR)
ClinVar RCV:
RCV000008672
RCV001777133
ClinVar Variation:
8190
dbSNP:
41469351
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370771C>T , CM000665.2:g.46370771C>T GRCh38
NC_000003.11:g.46412262C>T , CM000665.1:g.46412262C>T GRCh37
NC_000003.10:g.46387266C>T NCBI36
NG_012637.1:g.5630C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000579.3:c.-229C>T (CCR5) NP_000570.1:n.-229C>T
NM_001100168.1:c.-65-164C>T (CCR5) NP_001093638.1:n.-65-164C>T
NR_125406.1:n.565+473G>A (CCR5AS)
NM_000579.4:c.-229C>T (CCR5) NP_000570.1:n.-229C>T
NM_001100168.2:c.-65-164C>T (CCR5) NP_001093638.1:n.-65-164C>T
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