Canonical Allele Identifier: CA337625450

Gene:

Linked Data

• dbSNP Id: rs13305141
• MyVariant Identifiers: chrY:g.8575957T>A (hg19) ; chrY:g.8707916T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.8707916T>A , CM000686.2:g.8707916T>A	GRCh38
NC_000024.9:g.8575957T>A , CM000686.1:g.8575957T>A	GRCh37
NC_000024.8:g.8635957T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000623558.1:c.139+8884T>A	ENSP00000485446.1:n.139+8884T>A
ENST00000624593.1:c.-57+40800A>T	ENSP00000485106.1:n.-57+40800A>T