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 17:65536345 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 12342

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

17:g.65536345C>A
ENST00000618960.2:c.1921G>T
ENSP00000478916.1:p.Glu641Ter
ENST00000375702.5:c.1921G>T
ENSP00000364854.5:p.Glu641Ter
ENST00000578251.1:n.338G>T
ENST00000307078.7:c.2116G>T
ENSP00000302625.5:p.Glu706Ter
ENST00000611991.1:c.397-7645G>T
LRG_296:g.30278G>T
LRG_296t1.1:c.2116G>T
LRG_296p1.1:p.Glu706Ter

Variation displays