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 19:39507456 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM031160

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11452, 2010_April_001_032_DLL3_602768_0008

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

19:g.39507456G>A
ENST00000205143.4:c.1511G>A
ENSP00000205143.3:p.Gly504Asp
ENST00000356433.7:c.1511G>A
ENSP00000348810.4:p.Gly504Asp

Variation displays