Canonical Allele Identifier: CA433593449
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414861T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373370T>G , CM000665.2:g.46373370T>G GRCh38
NC_000003.11:g.46414861T>G , CM000665.1:g.46414861T>G GRCh37
NC_000003.10:g.46389865T>G NCBI36
NG_012637.1:g.8229T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.468T>G ENSP00000292303.4:p.Ala156=
ENST00000445772.1:c.468T>G ENSP00000404881.1:p.Ala156=
NM_000579.3:c.468T>G NP_000570.1:p.Ala156=
NM_001100168.1:c.468T>G NP_001093638.1:p.Ala156=
NM_000579.4:c.468T>G NP_000570.1:p.Ala156=
NM_001100168.2:c.468T>G NP_001093638.1:p.Ala156=