Canonical Allele Identifier: CA414941376
Gene: SRY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787318A>G , CM000686.2:g.2787318A>G GRCh38
NC_000024.9:g.2655359A>G , CM000686.1:g.2655359A>G GRCh37
NC_000024.8:g.2715359A>G NCBI36
NG_011751.1:g.5434T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12579A>G
ENST00000679825.1:n.430A>G
ENST00000680285.1:n.320-2431A>G
ENST00000680845.1:n.166-162A>G
ENST00000681787.1:n.106+12579A>G
ENST00000681940.1:n.106+12579A>G
ENST00000383070.2:c.286T>C MANE Select ENSP00000372547.1:p.Tyr96His
ENST00000383070.1:c.286T>C ENSP00000372547.1:p.Tyr96His
NM_003140.2:c.286T>C NP_003131.1:p.Tyr96His
NM_003140.3:c.286T>C MANE Select NP_003131.1:p.Tyr96His