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 2:97737828 (forward strand) | View in location tab

Co-located
Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_137_ZAP70_176947_0003, 5039

This variation has 12 HGVS names - click the plus to show

2:g.97737828C>A
ENST00000487283.2:n.2606C>A
ENST00000495754.1:n.492C>A
ENST00000451498.2:c.633C>A
ENSP00000400475.2:p.Ser211Arg
ENST00000463643.2:n.1415C>A
ENST00000264972.6:c.1554C>A
ENSP00000264972.5:p.Ser518Arg
ENST00000489250.1:n.7C>A
LRG_126:g.29261C>A
LRG_126t1.1:c.1554C>A
LRG_126p1.1:p.Ser518Arg

Variation displays