Canonical Allele Identifier: CA907590168

Linked Data

dbSNP Id: rs1309914204
gnomAD v3: 3-46370395-T-G
gnomAD v4: 3-46370395-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370395T>G , CM000665.2:g.46370395T>G GRCh38
NC_000003.11:g.46411886T>G , CM000665.1:g.46411886T>G GRCh37
NC_000003.10:g.46386890T>G NCBI36
NG_012637.1:g.5254T>G

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+197T>G (CCR5) NP_000570.1:n.-301+197T>G
NM_001100168.1:c.-66+197T>G (CCR5) NP_001093638.1:n.-66+197T>G
NR_125406.1:n.565+849A>C (CCR5AS)
NM_000579.4:c.-301+197T>G (CCR5) NP_000570.1:n.-301+197T>G
NM_001100168.2:c.-66+197T>G (CCR5) NP_001093638.1:n.-66+197T>G