Canonical Allele Identifier: CA73685345

Linked Data

dbSNP Id: rs778034886

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373497G>A , CM000665.2:g.46373497G>A GRCh38
NC_000003.11:g.46414988G>A , CM000665.1:g.46414988G>A GRCh37
NC_000003.10:g.46389992G>A NCBI36
NG_012637.1:g.8356G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.595G>A (CCR5) MANE Select ENSP00000292303.4:p.Val199Ile
ENST00000292303.4:c.595G>A (CCR5) ENSP00000292303.4:p.Val199Ile
ENST00000445772.1:c.595G>A (CCR5) ENSP00000404881.1:p.Val199Ile
NM_000579.3:c.595G>A (CCR5) NP_000570.1:p.Val199Ile
NM_001100168.1:c.595G>A (CCR5) NP_001093638.1:p.Val199Ile
NR_125406.1:n.392-2080C>T (CCR5AS)
NM_000579.4:c.595G>A (CCR5) NP_000570.1:p.Val199Ile
NM_001100168.2:c.595G>A (CCR5) NP_001093638.1:p.Val199Ile
NM_001394783.1:c.595G>A (CCR5) MANE Select NP_001381712.1:p.Val199Ile