Canonical Allele Identifier: CA337437892

Gene: SRY

Linked Data

• dbSNP Id: rs947193756
• gnomAD v3: Y-2787688-A-T
• gnomAD v4: Y-2787688-A-T
• MyVariant Identifiers: chrY:g.2655729A>T (hg19) ; chrY:g.2787688A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787688A>T , CM000686.2:g.2787688A>T	GRCh38
NC_000024.9:g.2655729A>T , CM000686.1:g.2655729A>T	GRCh37
NC_000024.8:g.2715729A>T	NCBI36
NG_011751.1:g.5064T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000679518.1:n.106+12949A>T
ENST00000680285.1:n.320-2061A>T
ENST00000681787.1:n.106+12949A>T
ENST00000681940.1:n.106+12949A>T
ENST00000383070.1:c.-85T>A	ENSP00000372547.1:n.-85T>A
NM_003140.2:c.-85T>A	NP_003131.1:n.-85T>A