Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 19:41848114 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002414

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5753, 2010_April_001_104_TGFB1_190180_0001, NM_000660.4:c.673T>C

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

19:g.41848114A>G
ENST00000597453.1:n.204T>C
ENST00000221930.5:c.673T>C
ENSP00000221930.4:p.Cys225Arg
ENST00000600196.1:n.133T>C

Variation displays