ClinGen Allele Registry
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Canonical Allele Identifier:
CA337517847
Gene: TUSC2P1
HGNC
NCBI
Linked Data
dbSNP Id:
rs2566671
gnomAD v3:
Y-5887509-T-C
gnomAD v4:
Y-5887509-T-C
MyVariant Identifiers:
chrY:g.5755550T>C (hg19)
chrY:g.5887509T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.5887509T>C , CM000686.2:g.5887509T>C
GRCh38
NC_000024.9:g.5755550T>C , CM000686.1:g.5755550T>C
GRCh37
NC_000024.8:g.5815550T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000645906.1:n.6T>C
Search 100 bp 5'
Search 100 bp 3'