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 13:110155300 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM090727

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_001845.4:c.4738G>C, 965

This variation has 3 HGVS names - click the plus to show

13:g.110155300C>G
ENST00000375820.6:c.4738G>C
ENSP00000364979.4:p.Gly1580Arg

Variation displays