Original source

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

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

Chromosome X:107642415 (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 9 HGVS names - click the plus to show

X:g.107642415T>C
ENST00000372418.2:c.155T>C
ENSP00000361495.1:p.Leu52Pro
ENST00000372435.5:c.455T>C
ENSP00000361512.4:p.Leu152Pro
ENST00000372428.5:c.-82-2762T>C
LRG_264:g.18992T>C
LRG_264t1.1:c.455T>C
LRG_264p1.1:p.Leu152Pro

Variation displays