Canonical Allele Identifier: CA2354529

Linked Data

dbSNP Id: rs775290065
gnomAD v2: 3-46414380-C-T
gnomAD v4: 3-46372889-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372889C>T , CM000665.2:g.46372889C>T GRCh38
NC_000003.11:g.46414380C>T , CM000665.1:g.46414380C>T GRCh37
NC_000003.10:g.46389384C>T NCBI36
NG_012637.1:g.7748C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.-11-3C>T (CCR5) MANE Select ENSP00000292303.4:n.-11-3C>T
ENST00000292303.4:c.-11-3C>T (CCR5) ENSP00000292303.4:n.-11-3C>T
ENST00000445772.1:c.-14C>T (CCR5) ENSP00000404881.1:n.-14C>T
NM_000579.3:c.-11-3C>T (CCR5) NP_000570.1:n.-11-3C>T
NM_001100168.1:c.-11-3C>T (CCR5) NP_001093638.1:n.-11-3C>T
NR_125406.1:n.392-1472G>A (CCR5AS)
NM_000579.4:c.-11-3C>T (CCR5) NP_000570.1:n.-11-3C>T
NM_001100168.2:c.-11-3C>T (CCR5) NP_001093638.1:n.-11-3C>T
NM_001394783.1:c.-11-3C>T (CCR5) MANE Select NP_001381712.1:n.-11-3C>T