Canonical Allele Identifier: CA519429403
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655030C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2786989C>T , CM000686.2:g.2786989C>T GRCh38
NC_000024.9:g.2655030C>T , CM000686.1:g.2655030C>T GRCh37
NC_000024.8:g.2715030C>T NCBI36
NG_011751.1:g.5763G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+12250C>T
ENST00000679825.1:n.107-6C>T
ENST00000680285.1:n.320-2760C>T
ENST00000680845.1:n.107-6C>T
ENST00000681787.1:n.106+12250C>T
ENST00000681940.1:n.106+12250C>T
ENST00000383070.2:c.615G>A MANE Select ENSP00000372547.1:p.Ter205=
ENST00000383070.1:c.615G>A ENSP00000372547.1:p.Ter205=
NM_003140.2:c.615G>A NP_003131.1:p.Ter205=
NM_003140.3:c.615G>A MANE Select NP_003131.1:p.Ter205=