Canonical Allele Identifier: CA433593419
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414846C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373355C>T , CM000665.2:g.46373355C>T GRCh38
NC_000003.11:g.46414846C>T , CM000665.1:g.46414846C>T GRCh37
NC_000003.10:g.46389850C>T NCBI36
NG_012637.1:g.8214C>T

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.453C>T NP_000570.1:p.Ile151=
NM_001100168.1:c.453C>T NP_001093638.1:p.Ile151=
NR_125406.1:n.392-1938G>A
NM_000579.4:c.453C>T NP_000570.1:p.Ile151=
NM_001100168.2:c.453C>T NP_001093638.1:p.Ile151=
ENST00000292303.4:c.453C>T ENSP00000292303.4:p.Ile151=
ENST00000445772.1:c.453C>T ENSP00000404881.1:p.Ile151=