Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C/G|Ancestral: A|Ambiguity code: V
Location

Chromosome 16:176745 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM086364 ; PhenCode HbVar.2594 (A/G)

Most severe consequence
 
Missense variant
Synonyms

LSDB HbVar.2594, HbVar.1239_1

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and 1 regulatory feature.

Variant displays