Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/G | Ambiguity code: S
Location

Chromosome Y:2655362 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930699

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8621, 2010_April_001_013_SRY_480000_0016

This variation has 7 HGVS names - click the plus to show

Y:g.2655362C>G
ENST00000534739.2:c.283G>C
ENSP00000438917.1:p.Gly95Arg
ENST00000525526.2:c.283G>C
ENSP00000437575.1:p.Gly95Arg
ENST00000383070.1:c.283G>C
ENSP00000372547.1:p.Gly95Arg

Variation displays