Canonical Allele Identifier: CA519724218
Gene: SRY HGNC NCBI

Linked Data

dbSNP Id: rs2124486304
MyVariant Identifiers: chrY:g.2655459T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787418T>A , CM000686.2:g.2787418T>A GRCh38
NC_000024.9:g.2655459T>A , CM000686.1:g.2655459T>A GRCh37
NC_000024.8:g.2715459T>A NCBI36
NG_011751.1:g.5334A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12679T>A
ENST00000679825.1:n.530T>A
ENST00000680285.1:n.320-2331T>A
ENST00000680845.1:n.166-62T>A
ENST00000681787.1:n.106+12679T>A
ENST00000681940.1:n.106+12679T>A
ENST00000383070.2:c.186A>T MANE Select ENSP00000372547.1:p.Arg62=
ENST00000383070.1:c.186A>T ENSP00000372547.1:p.Arg62=
NM_003140.2:c.186A>T NP_003131.1:p.Arg62=
NM_003140.3:c.186A>T MANE Select NP_003131.1:p.Arg62=