Canonical Allele Identifier: CA519770562
Gene: MXRA5Y HGNC NCBI

Linked Data

dbSNP Id: rs1603163482
MyVariant Identifiers: chrY:g.14077917C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.11957211C>T , CM000686.2:g.11957211C>T GRCh38
NC_000024.9:g.14077917C>T , CM000686.1:g.14077917C>T GRCh37
NC_000024.8:g.12587917C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000420610.1:n.4C>T