Canonical Allele Identifier:
CA519539834
Gene:
Linked Data
dbSNP Id:
rs2014116491
gnomAD v3:
Y-7680842-C-A
gnomAD v4:
Y-7680842-C-A
MyVariant Identifiers:
chrY:g.7548883C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.7680842C>A , CM000686.2:g.7680842C>A | GRCh38 |
| NC_000024.9:g.7548883C>A , CM000686.1:g.7548883C>A | GRCh37 |
| NC_000024.8:g.7608883C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439805.1:n.594C>A |