Canonical Allele Identifier: CA433593427
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414849T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373358T>G , CM000665.2:g.46373358T>G GRCh38
NC_000003.11:g.46414849T>G , CM000665.1:g.46414849T>G GRCh37
NC_000003.10:g.46389853T>G NCBI36
NG_012637.1:g.8217T>G

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.456T>G NP_000570.1:p.Thr152=
NM_001100168.1:c.456T>G NP_001093638.1:p.Thr152=
NR_125406.1:n.392-1941A>C
NM_000579.4:c.456T>G NP_000570.1:p.Thr152=
NM_001100168.2:c.456T>G NP_001093638.1:p.Thr152=
ENST00000292303.4:c.456T>G ENSP00000292303.4:p.Thr152=
ENST00000445772.1:c.456T>G ENSP00000404881.1:p.Thr152=