Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 13:103504594 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 1784

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

13:g.103504594C>A
ENST00000602836.1:c.1491C>A
ENSP00000473384.1:p.Pro498His
ENST00000355739.4:c.215C>A
ENSP00000347978.4:p.Pro72His
ENST00000535557.1:c.215C>A
ENSP00000442117.1:p.Pro72His
ENST00000472151.1:c.*120C>A
ENST00000375958.3:n.370C>A
LRG_464:g.11421C>A
LRG_464t1.1:c.215C>A
LRG_464p1.1:p.Pro72His

Variation displays