Canonical Allele Identifier: CA337553369
Gene: RBMY1KP HGNC NCBI

Linked Data

dbSNP Id: rs373796463
MyVariant Identifiers: chrY:g.24359935A>G (hg19) chrY:g.22213788A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.22213788A>G , CM000686.2:g.22213788A>G GRCh38
NC_000024.9:g.24359935A>G , CM000686.1:g.24359935A>G GRCh37
NC_000024.8:g.22769323A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423480.1:n.361+1187A>G
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