Canonical Allele Identifier: CA907590144

Linked Data

dbSNP Id: rs1317679609
gnomAD v3: 3-46370376-T-G
gnomAD v4: 3-46370376-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370376T>G , CM000665.2:g.46370376T>G GRCh38
NC_000003.11:g.46411867T>G , CM000665.1:g.46411867T>G GRCh37
NC_000003.10:g.46386871T>G NCBI36
NG_012637.1:g.5235T>G

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+178T>G (CCR5) NP_000570.1:n.-301+178T>G
NM_001100168.1:c.-66+178T>G (CCR5) NP_001093638.1:n.-66+178T>G
NR_125406.1:n.565+868A>C (CCR5AS)
NM_000579.4:c.-301+178T>G (CCR5) NP_000570.1:n.-301+178T>G
NM_001100168.2:c.-66+178T>G (CCR5) NP_001093638.1:n.-66+178T>G