Original source

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

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

Chromosome 19:33302164 (forward strand) | View in location tab

Co-located

with COSMIC COSM1378 (T/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_017_CEBPA_116897_0003, 807

This variation has 6 HGVS names - click the plus to show

19:g.33302164T>A
ENST00000498907.2:c.251A>T
ENSP00000427514.1:p.His84Leu
LRG_456:g.5361A>T
LRG_456t1:c.251A>T
LRG_456p1:p.His84Leu

Variation displays