Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 6:73638477 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM993212

Most severe consequence
Clinical significance

Synonyms

LSDB 12594

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

6:g.73638477T>C
ENST00000355773.5:c.548A>G
ENSP00000348019.5:p.His183Arg
ENST00000481996.1:n.314A>G

Variation displays