Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 1:229433109 (forward strand) | View in location tab

Co-located

with COSMIC COSM3385880 (C/T) ; HGMD-PUBLIC CM042925 ; PhenCode ACTA1:c.7G>T (C/A)

Most severe consequence
Clinical significance

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

1:g.229433109C>A
ENST00000366683.3:c.7G>T
ENSP00000355644.3:p.Asp3Tyr
ENST00000366684.5:c.7G>T
ENSP00000355645.3:p.Asp3Tyr

Variation displays