Canonical Allele Identifier: CA519724521
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655360T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787319T>G , CM000686.2:g.2787319T>G GRCh38
NC_000024.9:g.2655360T>G , CM000686.1:g.2655360T>G GRCh37
NC_000024.8:g.2715360T>G NCBI36
NG_011751.1:g.5433A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12580T>G
ENST00000679825.1:n.431T>G
ENST00000680285.1:n.320-2430T>G
ENST00000680845.1:n.166-161T>G
ENST00000681787.1:n.106+12580T>G
ENST00000681940.1:n.106+12580T>G
ENST00000383070.2:c.285A>C MANE Select ENSP00000372547.1:p.Gly95=
ENST00000383070.1:c.285A>C ENSP00000372547.1:p.Gly95=
NM_003140.2:c.285A>C NP_003131.1:p.Gly95=
NM_003140.3:c.285A>C MANE Select NP_003131.1:p.Gly95=