Canonical Allele Identifier: CA519540009

Gene:

Linked Data

• MyVariant Identifiers: chrY:g.7548898T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.7680857T>G , CM000686.2:g.7680857T>G	GRCh38
NC_000024.9:g.7548898T>G , CM000686.1:g.7548898T>G	GRCh37
NC_000024.8:g.7608898T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439805.1:n.609T>G