Canonical Allele Identifier: CA73681892

Linked Data

dbSNP Id: rs1029021182
gnomAD v2: 3-46411868-G-T
gnomAD v3: 3-46370377-G-T
gnomAD v4: 3-46370377-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370377G>T , CM000665.2:g.46370377G>T GRCh38
NC_000003.11:g.46411868G>T , CM000665.1:g.46411868G>T GRCh37
NC_000003.10:g.46386872G>T NCBI36
NG_012637.1:g.5236G>T

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+179G>T (CCR5) NP_000570.1:n.-301+179G>T
NM_001100168.1:c.-66+179G>T (CCR5) NP_001093638.1:n.-66+179G>T
NR_125406.1:n.565+867C>A (CCR5AS)
NM_000579.4:c.-301+179G>T (CCR5) NP_000570.1:n.-301+179G>T
NM_001100168.2:c.-66+179G>T (CCR5) NP_001093638.1:n.-66+179G>T