Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Y:2787320 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM004706

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_018_SRY_480000_0022, 8627

This variation has 5 HGVS names - click the plus to show

Y:g.2787320C>T
ENST00000623823.1:c.284G>A
ENSP00000485519.1:p.Gly95Glu
ENST00000383070.1:c.284G>A
ENSP00000372547.1:p.Gly95Glu

Variation displays