ClinGen Allele Registry
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Canonical Allele Identifier:
CA337514336
Gene:
Linked Data
dbSNP Id:
rs111377238
MyVariant Identifiers:
chrY:g.23005170C>T (hg19)
chrY:g.20843284C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.20843284C>T , CM000686.2:g.20843284C>T
GRCh38
NC_000024.9:g.23005170C>T , CM000686.1:g.23005170C>T
GRCh37
NC_000024.8:g.21414558C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000406090.1:n.427G>A
Search 100 bp 5'
Search 100 bp 3'