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 19:39507099 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000506

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11447, 2010_April_001_030_DLL3_602768_0003

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

19:g.39507099G>A
ENST00000596614.2:c.470G>A
ENSP00000471688.1:p.Gly157Asp
ENST00000205143.4:c.1154G>A
ENSP00000205143.3:p.Gly385Asp
ENST00000356433.6:c.1154G>A
ENSP00000348810.4:p.Gly385Asp

Variation displays