Canonical Allele Identifier: CA337645440

Gene: RBMY2QP

Linked Data

• dbSNP Id: rs13304762
• MyVariant Identifiers: chrY:g.9819252C>G (hg19) ; chrY:g.9981643C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.9981643C>G , CM000686.2:g.9981643C>G	GRCh38
NC_000024.9:g.9819252C>G , CM000686.1:g.9819252C>G	GRCh37
NC_000024.8:g.10429252C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651645.1:n.1003+7547G>C