ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA337767953
Gene:
Linked Data
dbSNP Id:
rs112501714
gnomAD v3:
Y-15291856-G-A
gnomAD v4:
Y-15291856-G-A
MyVariant Identifiers:
chrY:g.17403736G>A (hg19)
chrY:g.15291856G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15291856G>A , CM000686.2:g.15291856G>A
GRCh38
NC_000024.9:g.17403736G>A , CM000686.1:g.17403736G>A
GRCh37
NC_000024.8:g.15913130G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
XR_001756089.1:n.310-44678C>T
Search 100 bp 5'
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