Canonical Allele Identifier: CA414941380

Gene: SRY

Linked Data

• dbSNP Id: rs104894974
• MyVariant Identifiers: chrY:g.2655362C>A (hg19) ; chrY:g.2787321C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.2787321C>A , CM000686.2:g.2787321C>A	GRCh38
NC_000024.9:g.2655362C>A , CM000686.1:g.2655362C>A	GRCh37
NC_000024.8:g.2715362C>A	NCBI36
NG_011751.1:g.5431G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679518.1:n.106+12582C>A
ENST00000679825.1:n.433C>A
ENST00000680285.1:n.320-2428C>A
ENST00000680845.1:n.166-159C>A
ENST00000681787.1:n.106+12582C>A
ENST00000681940.1:n.106+12582C>A
ENST00000383070.2:c.283G>T MANE Select	ENSP00000372547.1:p.Gly95Ter
ENST00000383070.1:c.283G>T	ENSP00000372547.1:p.Gly95Ter
NM_003140.2:c.283G>T	NP_003131.1:p.Gly95Ter
NM_003140.3:c.283G>T MANE Select	NP_003131.1:p.Gly95Ter