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 10:13283713 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971175

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_072_PHYH_602026_0004, 10730

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

10:g.13283713T>G
ENST00000396913.4:c.505A>C
ENSP00000380121.2:p.Asn169His
ENST00000453759.4:c.505A>C
ENSP00000412525.2:p.Asn169His
ENST00000396920.5:c.754A>C
ENSP00000380126.3:p.Asn252His
ENST00000263038.6:c.805A>C
ENSP00000263038.4:p.Asn269His

Variation displays