Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 5:60902446 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043839

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

5:g.60902446C>G
ENST00000265038.6:c.613G>C
ENSP00000265038.5:p.Ala205Pro
ENST00000495985.2:n.390G>C
ENST00000484330.2:n.289G>C
ENST00000462279.2:n.458G>C
ENST00000381118.4:c.*657G>C
LRG_466:g.47633G>C
LRG_466t1.1:c.613G>C
LRG_466p1.1:p.Ala205Pro

Variation displays