Canonical Allele Identifier: CA880376495
Gene: RBMY1KP HGNC NCBI

Linked Data

dbSNP Id: rs1431935431
MyVariant Identifiers: chrY:g.24359855C>T (hg19) chrY:g.22213708C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.22213708C>T , CM000686.2:g.22213708C>T GRCh38
NC_000024.9:g.24359855C>T , CM000686.1:g.24359855C>T GRCh37
NC_000024.8:g.22769243C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423480.1:n.361+1107C>T
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