Canonical Allele Identifier: CA254884
Gene: SRY HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 9753
ClinVar RCV Id: RCV000010407
dbSNP Id: rs104894977

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787600G>A , CM000686.2:g.2787600G>A GRCh38
NC_000024.9:g.2655641G>A , CM000686.1:g.2655641G>A GRCh37
NC_000024.8:g.2715641G>A NCBI36
NG_011751.1:g.5152C>T

Transcript Alleles

HGVS Amino-acid change
NM_003140.2:c.4C>T VV NP_003131.1:p.Gln2Ter
ENST00000383070.1:c.4C>T ENSP00000372547.1:p.Gln2Ter