This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
C/A/T|Ambiguity code: H
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms

LSDB NG_029922.1:g.11284G>A, NG_029922.1:g.11284G>T

HGVS name

None

Variant displays