Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 6:121446908 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030453

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1373, 2010_April_001_062_GJA1_121014_0005

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

6:g.121446908G>A
ENST00000282561.3:c.61G>A
ENSP00000282561.3:p.Gly21Arg

Variation displays