Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.39 (T)
Location

Chromosome 6:166579270 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

6:g.166579270C>T
ENST00000461348.2:c.530G>A
ENSP00000453512.1:p.Gly177Asp
ENST00000296946.2:c.530G>A
ENSP00000296946.2:p.Gly177Asp
ENST00000366871.3:c.530G>A
ENSP00000355836.3:p.Gly177Asp
ENST00000366876.2:c.530G>A
ENSP00000355841.2:p.Gly177Asp

This variation has assays on 9 chips - click the plus to show

Variation displays