Canonical Allele Identifier: CA1047499304

Linked Data

dbSNP Id: rs1701643244
gnomAD v3: 3-46370185-G-A
gnomAD v4: 3-46370185-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370185G>A , CM000665.2:g.46370185G>A GRCh38
NC_000003.11:g.46411676G>A , CM000665.1:g.46411676G>A GRCh37
NC_000003.10:g.46386680G>A NCBI36
NG_012637.1:g.5044G>A

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-314G>A (CCR5) NP_000570.1:n.-314G>A
NM_001100168.1:c.-79G>A (CCR5) NP_001093638.1:n.-79G>A
NR_125406.1:n.565+1059C>T (CCR5AS)
NM_000579.4:c.-314G>A (CCR5) NP_000570.1:n.-314G>A
NM_001100168.2:c.-79G>A (CCR5) NP_001093638.1:n.-79G>A