Canonical Allele Identifier: CA519593598
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775190T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907149T>G , CM000686.2:g.8907149T>G GRCh38
NC_000024.9:g.8775190T>G , CM000686.1:g.8775190T>G GRCh37
NC_000024.8:g.8835190T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.165T>G