Canonical Allele Identifier: CA352471294

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373375T>C , CM000665.2:g.46373375T>C GRCh38
NC_000003.11:g.46414866T>C , CM000665.1:g.46414866T>C GRCh37
NC_000003.10:g.46389870T>C NCBI36
NG_012637.1:g.8234T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.473T>C (CCR5) MANE Select ENSP00000292303.4:p.Phe158Ser
ENST00000292303.4:c.473T>C (CCR5) ENSP00000292303.4:p.Phe158Ser
ENST00000445772.1:c.473T>C (CCR5) ENSP00000404881.1:p.Phe158Ser
NM_000579.3:c.473T>C (CCR5) NP_000570.1:p.Phe158Ser
NM_001100168.1:c.473T>C (CCR5) NP_001093638.1:p.Phe158Ser
NR_125406.1:n.392-1958A>G (CCR5AS)
NM_000579.4:c.473T>C (CCR5) NP_000570.1:p.Phe158Ser
NM_001100168.2:c.473T>C (CCR5) NP_001093638.1:p.Phe158Ser
NM_001394783.1:c.473T>C (CCR5) MANE Select NP_001381712.1:p.Phe158Ser