Canonical Allele Identifier: CA337645442
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs13304073
MyVariant Identifiers: chrY:g.9819254G>T (hg19) chrY:g.9981645G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981645G>T , CM000686.2:g.9981645G>T GRCh38
NC_000024.9:g.9819254G>T , CM000686.1:g.9819254G>T GRCh37
NC_000024.8:g.10429254G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.1003+7545C>A
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