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 15:66436843 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061104

Most severe consequence
Clinical significance

Synonyms

LSDB 4944

This variation has 4 HGVS names - click the plus to show

15:g.66436843A>G
ENST00000307102.7:c.389A>G
ENSP00000302486.4:p.Tyr130Cys
ENST00000425818.2:n.900A>G

Variation displays