Original source

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

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

Chromosome 8:43033327 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065270

Most severe consequence
Clinical significance

Synonyms

LSDB 16745

This variation has 9 HGVS names - click the plus to show

8:g.43033327T>G
ENST00000522082.1:c.203T>G
ENSP00000430151.1:p.Leu68Ter
ENST00000458501.2:c.1046T>G
ENSP00000389524.2:p.Leu349Ter
ENST00000379644.4:c.962T>G
ENSP00000368965.4:p.Leu321Ter
ENST00000524016.1:c.66T>G
ENSP00000428322.1:p.Leu23Ter

Variation displays