Canonical Allele Identifier: CA10587409

Gene:

Linked Data

• dbSNP Id: rs886038301
• MyVariant Identifiers: chrY:g.541905A>T (hg19) ; chrY:g.631170A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.631170A>T , CM000686.2:g.631170A>T	GRCh38
NC_000024.9:g.541905A>T , CM000686.1:g.541905A>T	GRCh37
NC_000024.8:g.511905A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711141.1:c.273A>T	ENSP00000518639.1:p.Ala91=
ENST00000711142.1:c.273A>T	ENSP00000518640.1:p.Ala91=
ENST00000711143.1:c.273A>T	ENSP00000518641.1:p.Ala91=
ENST00000711145.1:c.273A>T	ENSP00000518642.1:p.Ala91=