Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:41848134 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002413

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000660.4:c.653G>A, 2010_April_001_105_TGFB1_190180_0002, 5754

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

19:g.41848134C>T
ENST00000597453.1:n.184G>A
ENST00000221930.5:c.653G>A
ENSP00000221930.4:p.Arg218His
ENST00000600196.1:n.113G>A

Variation displays