Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 11:124875150 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041430

Most severe consequence
Clinical significance

Synonyms

LSDB 15851

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

11:g.124875150T>C
ENST00000397801.3:c.2113T>C
ENSP00000380903.1:p.Ser705Pro
ENST00000538940.3:c.2047T>C
ENSP00000441797.1:p.Ser683Pro

Variation displays