Canonical Allele Identifier: CA1362081235

Linked Data

dbSNP Id: rs2734648

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370349G>C , CM000665.2:g.46370349G>C GRCh38
NC_000003.11:g.46411840G>C , CM000665.1:g.46411840G>C GRCh37
NC_000003.10:g.46386844G>C NCBI36
NG_012637.1:g.5208G>C

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+151G>C (CCR5) NP_000570.1:n.-301+151G>C
NM_001100168.1:c.-66+151G>C (CCR5) NP_001093638.1:n.-66+151G>C
NR_125406.1:n.565+895C>G (CCR5AS)
NM_000579.4:c.-301+151G>C (CCR5) NP_000570.1:n.-301+151G>C
NM_001100168.2:c.-66+151G>C (CCR5) NP_001093638.1:n.-66+151G>C