Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 6:43604646 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM994136

Most severe consequence
Clinical significance

Synonyms

LSDB 12331

This variation has 8 HGVS names - click the plus to show

6:g.43604646G>T
ENST00000372226.1:c.916G>T
ENSP00000361300.1:p.Glu306Ter
ENST00000372236.5:c.916G>T
ENSP00000361310.4:p.Glu306Ter
LRG_470:g.33506G>T
LRG_470t1.1:c.916G>T
LRG_470p1.1:p.Glu306Ter

Variation displays