Canonical Allele Identifier: CA254872
Gene: SRY HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9745
ClinVar RCV Id: RCV000010399
dbSNP Id: rs104894967

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787284C>T , CM000686.2:g.2787284C>T GRCh38
NC_000024.9:g.2655325C>T , CM000686.1:g.2655325C>T GRCh37
NC_000024.8:g.2715325C>T NCBI36
NG_011751.1:g.5468G>A

Transcript Alleles

HGVS Amino-acid change
NM_003140.2:c.320G>A VV NP_003131.1:p.Trp107Ter
ENST00000383070.1:c.320G>A ENSP00000372547.1:p.Trp107Ter