Canonical Allele Identifier: CA337438219

Gene:

Linked Data

• dbSNP Id: rs901687202
• MyVariant Identifiers: chrY:g.2668424G>C (hg19) ; chrY:g.2800383G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2800383G>C , CM000686.2:g.2800383G>C	GRCh38
NC_000024.9:g.2668424G>C , CM000686.1:g.2668424G>C	GRCh37
NC_000024.8:g.2728424G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+25644G>C
ENST00000681787.1:n.106+25644G>C
ENST00000681940.1:n.106+25644G>C