Canonical Allele Identifier: CA433593584
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414873T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373382T>C , CM000665.2:g.46373382T>C GRCh38
NC_000003.11:g.46414873T>C , CM000665.1:g.46414873T>C GRCh37
NC_000003.10:g.46389877T>C NCBI36
NG_012637.1:g.8241T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.480T>C ENSP00000292303.4:p.Ser160=
ENST00000445772.1:c.480T>C ENSP00000404881.1:p.Ser160=
NM_000579.3:c.480T>C NP_000570.1:p.Ser160=
NM_001100168.1:c.480T>C NP_001093638.1:p.Ser160=
NM_000579.4:c.480T>C NP_000570.1:p.Ser160=
NM_001100168.2:c.480T>C NP_001093638.1:p.Ser160=