Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 18:23556436 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM012422

Most severe consequence
Clinical significance

Synonyms

LSDB 15117

This variation has 6 HGVS names - click the plus to show

18:g.23556436A>G
ENST00000269228.7:c.1133T>C
ENSP00000269228.4:p.Val378Ala
ENST00000540608.3:n.1047T>C
ENST00000591051.1:c.415T>C
ENSP00000467636.1:p.Val139Ala

Variation displays