Original source

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

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

Chromosome 8:43178184 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065270

Most severe consequence
Clinical significance

Synonyms

LSDB 16745

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

8:g.43178184T>G
ENST00000522082.2:c.203T>G
ENSP00000430151.1:p.Leu68Ter
ENST00000379644.5:c.962T>G
ENSP00000368965.4:p.Leu321Ter
ENST00000524016.2:c.66T>G
ENSP00000428322.1:p.Leu23Ter

Variation displays