Original source

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

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

Chromosome 10:71732292 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030204

Most severe consequence
Clinical significance

Synonyms

LSDB 13251

This variation has 11 HGVS names - click the plus to show

10:g.71732292G>A
ENST00000616684.2:c.4156G>A
ENSP00000482036.1:p.Asp1386Asn
ENST00000398786.2:c.-6+5436C>T
ENST00000398809.6:c.4018G>A
ENSP00000381789.5:p.Asp1340Asn
ENST00000622827.2:c.4021G>A
ENSP00000483211.1:p.Asp1341Asn
ENST00000224721.8:c.4171G>A
ENSP00000224721.7:p.Asp1391Asn
ENST00000398792.3:n.713G>A

Variation displays