Original source

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

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

Chromosome 6:43587375 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM991064

Most severe consequence
Clinical significance

Synonyms

LSDB 12333

This variation has 10 HGVS names - click the plus to show

6:g.43587375C>T
ENST00000372226.1:c.376C>T
ENSP00000361300.1:p.Gln126Ter
ENST00000443535.1:c.190C>T
ENSP00000405320.1:p.Gln64Ter
ENST00000372236.5:c.376C>T
ENSP00000361310.4:p.Gln126Ter
LRG_470:g.16235C>T
LRG_470t1.1:c.376C>T
LRG_470p1.1:p.Gln126Ter

Variation displays