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 2:211456617 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012351

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

2:g.211456617A>G
ENST00000430249.2:c.1028A>G
ENSP00000402608.2:p.His343Arg
ENST00000233072.5:c.1010A>G
ENSP00000233072.5:p.His337Arg
LRG_336:g.119209A>G
LRG_336t1.1:c.1010A>G
LRG_336p1.1:p.His337Arg

Variation displays