Canonical Allele Identifier: CA2354551

Linked Data

dbSNP Id: rs768398484
gnomAD v2: 3-46414457-A-T
gnomAD v4: 3-46372966-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372966A>T , CM000665.2:g.46372966A>T GRCh38
NC_000003.11:g.46414457A>T , CM000665.1:g.46414457A>T GRCh37
NC_000003.10:g.46389461A>T NCBI36
NG_012637.1:g.7825A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.64A>T (CCR5) MANE Select ENSP00000292303.4:p.Lys22Ter
ENST00000292303.4:c.64A>T (CCR5) ENSP00000292303.4:p.Lys22Ter
ENST00000445772.1:c.64A>T (CCR5) ENSP00000404881.1:p.Lys22Ter
NM_000579.3:c.64A>T (CCR5) NP_000570.1:p.Lys22Ter
NM_001100168.1:c.64A>T (CCR5) NP_001093638.1:p.Lys22Ter
NR_125406.1:n.392-1549T>A (CCR5AS)
NM_000579.4:c.64A>T (CCR5) NP_000570.1:p.Lys22Ter
NM_001100168.2:c.64A>T (CCR5) NP_001093638.1:p.Lys22Ter
NM_001394783.1:c.64A>T (CCR5) MANE Select NP_001381712.1:p.Lys22Ter