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 17:63532463 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 12342

This variation has 9 HGVS names - click the plus to show

17:g.63532463C>A
ENST00000375702.5:c.1921G>T
ENSP00000364854.5:p.Glu641Ter
ENST00000578251.1:n.338G>T
ENST00000307078.5:c.2116G>T
ENSP00000302625.5:p.Glu706Ter
LRG_296:g.30278G>T
LRG_296t1.1:c.2116G>T
LRG_296p1.1:p.Glu706Ter

Variation displays