Canonical Allele Identifier: CA1362081240

Linked Data

dbSNP Id: rs1701645361

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370373T>C , CM000665.2:g.46370373T>C GRCh38
NC_000003.11:g.46411864T>C , CM000665.1:g.46411864T>C GRCh37
NC_000003.10:g.46386868T>C NCBI36
NG_012637.1:g.5232T>C

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+175T>C (CCR5) NP_000570.1:n.-301+175T>C
NM_001100168.1:c.-66+175T>C (CCR5) NP_001093638.1:n.-66+175T>C
NR_125406.1:n.565+871A>G (CCR5AS)
NM_000579.4:c.-301+175T>C (CCR5) NP_000570.1:n.-301+175T>C
NM_001100168.2:c.-66+175T>C (CCR5) NP_001093638.1:n.-66+175T>C