Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:106885645 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073282

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8433, NM_002764.3:c.455T>C

This variation has 12 HGVS names - click the plus to show

X:g.106885645T>C
ENST00000543248.1:c.455T>C
ENSP00000443185.1:p.Leu152Pro
ENST00000372418.1:c.155T>C
ENSP00000361495.1:p.Leu52Pro
ENST00000372435.4:c.455T>C
ENSP00000361512.4:p.Leu152Pro
ENST00000372428.4:c.254T>C
ENSP00000361505.4:p.Leu85Pro
LRG_264:g.18992T>C
LRG_264t1.1:c.455T>C
LRG_264p1.1:p.Leu152Pro

Variation displays