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 4:154589525 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM890186

Most severe consequence
Clinical significance

Synonyms

LSDB 1924

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

4:g.154589525C>A
ENST00000302053.4:c.92G>T
ENSP00000306361.3:p.Gly31Val
ENST00000403106.4:c.92G>T
ENSP00000385981.3:p.Gly31Val
ENST00000622532.1:c.92G>T
ENSP00000478487.1:p.Gly31Val
LRG_557:g.6221G>T
LRG_557t2.1:c.92G>T
LRG_557p2.1:p.Gly31Val
LRG_557t1.1:c.92G>T
LRG_557p1.1:p.Gly31Val

Variation displays