Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 19:40396207 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021124 ; PhenCode IPNMDB_570 (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13370, 2010_April_001_090_PRX_605725_0006, NM_181882.2:c.2145T>A

This variation has 8 HGVS names - click the plus to show

19:g.40396207A>T
ENST00000291825.9:c.*2350T>A
ENST00000324001.7:c.2145T>A
ENSP00000326018.6:p.Cys715Ter
LRG_265:g.22158T>A
LRG_265t2:c.2145T>A
LRG_265p2:p.Cys715Ter
LRG_265t1:c.*2350T>A

Variation displays