Canonical Allele Identifier: CA337533075

Gene:

Linked Data

• dbSNP Id: rs941516186
• MyVariant Identifiers: chrY:g.23479915A>G (hg19) ; chrY:g.21318029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.21318029A>G , CM000686.2:g.21318029A>G	GRCh38
NC_000024.9:g.23479915A>G , CM000686.1:g.23479915A>G	GRCh37
NC_000024.8:g.21889303A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437359.1:n.752+133A>G