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 13:110192257 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM076124

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001845.4:c.1493G>T, 961

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

13:g.110192257C>A
ENST00000375820.5:c.1493G>T
ENSP00000364979.4:p.Gly498Val
ENST00000543140.2:c.1493G>T
ENSP00000443348.1:p.Gly498Val

Variation displays