Canonical Allele Identifier: CA519724182
Gene: SRY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2655438C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2787397C>A , CM000686.2:g.2787397C>A GRCh38
NC_000024.9:g.2655438C>A , CM000686.1:g.2655438C>A GRCh37
NC_000024.8:g.2715438C>A NCBI36
NG_011751.1:g.5355G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+12658C>A
ENST00000679825.1:n.509C>A
ENST00000680285.1:n.320-2352C>A
ENST00000680845.1:n.166-83C>A
ENST00000681787.1:n.106+12658C>A
ENST00000681940.1:n.106+12658C>A
ENST00000383070.2:c.207G>T MANE Select ENSP00000372547.1:p.Val69=
ENST00000383070.1:c.207G>T ENSP00000372547.1:p.Val69=
NM_003140.2:c.207G>T NP_003131.1:p.Val69=
NM_003140.3:c.207G>T MANE Select NP_003131.1:p.Val69=