Canonical Allele Identifier: CA414941355
Gene: SRY HGNC NCBI

Linked Data

ClinVar Variation Id: 3040170
ClinVar RCV Id: RCV003924109
dbSNP Id: rs2124486099

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787310C>T , CM000686.2:g.2787310C>T GRCh38
NC_000024.9:g.2655351C>T , CM000686.1:g.2655351C>T GRCh37
NC_000024.8:g.2715351C>T NCBI36
NG_011751.1:g.5442G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12571C>T
ENST00000679825.1:n.422C>T
ENST00000680285.1:n.320-2439C>T
ENST00000680845.1:n.166-170C>T
ENST00000681787.1:n.106+12571C>T
ENST00000681940.1:n.106+12571C>T
ENST00000383070.2:c.294G>A MANE Select ENSP00000372547.1:p.Trp98Ter
ENST00000383070.1:c.294G>A ENSP00000372547.1:p.Trp98Ter
NM_003140.2:c.294G>A NP_003131.1:p.Trp98Ter
NM_003140.3:c.294G>A MANE Select NP_003131.1:p.Trp98Ter