Original source

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

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

Chromosome 11:47448145 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and 1 regulatory feature.

Variant displays