Canonical Allele Identifier: CA433593587
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414876C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373385C>G , CM000665.2:g.46373385C>G GRCh38
NC_000003.11:g.46414876C>G , CM000665.1:g.46414876C>G GRCh37
NC_000003.10:g.46389880C>G NCBI36
NG_012637.1:g.8244C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.483C>G ENSP00000292303.4:p.Leu161=
ENST00000445772.1:c.483C>G ENSP00000404881.1:p.Leu161=
NM_000579.3:c.483C>G NP_000570.1:p.Leu161=
NM_001100168.1:c.483C>G NP_001093638.1:p.Leu161=
NR_125406.1:n.392-1968G>C
NM_000579.4:c.483C>G NP_000570.1:p.Leu161=
NM_001100168.2:c.483C>G NP_001093638.1:p.Leu161=