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 13:102852244 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 1784

This variation has 14 HGVS names - click the plus to show

13:g.102852244C>A
ENST00000602836.1:c.1491C>A
ENSP00000473384.1:p.Pro498His
ENST00000535557.3:c.215C>A
ENSP00000442117.1:p.Pro72His
ENST00000355739.6:c.215C>A
ENSP00000347978.4:p.Pro72His
ENST00000472151.1:c.*120C>A
ENST00000610537.2:c.215C>A
ENSP00000478667.1:p.Pro72His
ENST00000375958.3:n.370C>A
LRG_464:g.11421C>A
LRG_464t1.1:c.215C>A
LRG_464p1.1:p.Gly78Arg

Variation displays