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Canonical Allele Identifier:
CA352471217
Gene: CCR5
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr3:g.46414848C>T (hg19)
chr3:g.46373357C>T (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.46373357C>T , CM000665.2:g.46373357C>T
GRCh38
NC_000003.11:g.46414848C>T , CM000665.1:g.46414848C>T
GRCh37
NC_000003.10:g.46389852C>T
NCBI36
NG_012637.1:g.8216C>T
Transcript Alleles
HGVS
Amino-acid change
NM_000579.3:c.455C>T
NP_000570.1:p.Thr152Ile
NM_001100168.1:c.455C>T
NP_001093638.1:p.Thr152Ile
NR_125406.1:n.392-1940G>A
NM_000579.4:c.455C>T
NP_000570.1:p.Thr152Ile
NM_001100168.2:c.455C>T
NP_001093638.1:p.Thr152Ile
ENST00000292303.4:c.455C>T
ENSP00000292303.4:p.Thr152Ile
ENST00000445772.1:c.455C>T
ENSP00000404881.1:p.Thr152Ile
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