Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 8:99784394 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041279

Most severe consequence
Clinical significance

Synonyms

LSDB 15257

This variation has 5 HGVS names - click the plus to show

8:g.99784394G>A
ENST00000358544.4:c.7934G>A
ENSP00000351346.2:p.Gly2645Asp
ENST00000357162.4:c.7859G>A
ENSP00000349685.2:p.Gly2620Asp

Variation displays