Original source

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

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

Chromosome 21:36461395 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM051892

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13321, 2009_August_001_005_CLDN14_605608_0003

This variation has 13 HGVS names - click the plus to show

21:g.36461395C>T
ENST00000399136.3:c.301G>A
ENSP00000382088.1:p.Gly101Arg
ENST00000342108.2:c.301G>A
ENSP00000339292.2:p.Gly101Arg
ENST00000428667.1:n.277+15388C>T
ENST00000399135.3:c.301G>A
ENSP00000382087.1:p.Gly101Arg
ENST00000399139.3:c.301G>A
ENSP00000382092.1:p.Gly101Arg
ENST00000429588.1:n.54-18836C>T
ENST00000399137.3:c.301G>A
ENSP00000382090.1:p.Gly101Arg

Variation displays