Canonical Allele Identifier: CA433593462
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414870G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373379G>T , CM000665.2:g.46373379G>T GRCh38
NC_000003.11:g.46414870G>T , CM000665.1:g.46414870G>T GRCh37
NC_000003.10:g.46389874G>T NCBI36
NG_012637.1:g.8238G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.477G>T ENSP00000292303.4:p.Ala159=
ENST00000445772.1:c.477G>T ENSP00000404881.1:p.Ala159=
NM_000579.3:c.477G>T NP_000570.1:p.Ala159=
NM_001100168.1:c.477G>T NP_001093638.1:p.Ala159=
NM_000579.4:c.477G>T NP_000570.1:p.Ala159=
NM_001100168.2:c.477G>T NP_001093638.1:p.Ala159=