Canonical Allele Identifier: CA337725469
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs2191146
MyVariant Identifiers: chrY:g.13090694C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13090694C>G , CM000686.2:g.13090694C>G GRCh38
NC_000024.8:g.13712002C>G NCBI36
NC_000024.9:g.15202608C>G , CM000686.1:g.15202608C>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000446621.1:n.556-3881C>G