Canonical Allele Identifier: CA2354656
Gene: CCR5 HGNC NCBI

Linked Data

dbSNP Id: rs746300015

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373378C>T , CM000665.2:g.46373378C>T GRCh38
NC_000003.11:g.46414869C>T , CM000665.1:g.46414869C>T GRCh37
NC_000003.10:g.46389873C>T NCBI36
NG_012637.1:g.8237C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.476C>T ENSP00000292303.4:p.Ala159Val
ENST00000445772.1:c.476C>T ENSP00000404881.1:p.Ala159Val
NM_000579.3:c.476C>T NP_000570.1:p.Ala159Val
NM_001100168.1:c.476C>T NP_001093638.1:p.Ala159Val
NM_000579.4:c.476C>T NP_000570.1:p.Ala159Val
NM_001100168.2:c.476C>T NP_001093638.1:p.Ala159Val