Canonical Allele Identifier: CA337645434

Gene: RBMY2QP

Linked Data

• dbSNP Id: rs903345537
• MyVariant Identifiers: chrY:g.9819193G>A (hg19) ; chrY:g.9981584G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.9981584G>A , CM000686.2:g.9981584G>A	GRCh38
NC_000024.9:g.9819193G>A , CM000686.1:g.9819193G>A	GRCh37
NC_000024.8:g.10429193G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651645.1:n.1003+7606C>T