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 11:64752071 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM994571

Most severe consequence
Clinical significance

Synonyms

LSDB 15734

This variation has 5 HGVS names - click the plus to show

11:g.64752071C>A
ENST00000164139.3:c.1621G>T
ENSP00000164139.3:p.Glu541Ter
ENST00000377432.5:c.1357G>T
ENSP00000366650.3:p.Glu453Ter

Variation displays