Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 2:26464868 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB DFNB9_42

This variation has 7 HGVS names - click the plus to show

2:g.26464868C>G
ENST00000464574.1:n.709+1G>C
ENST00000403946.5:c.4960+1G>C
ENST00000338581.8:c.2659+1G>C
ENST00000272371.4:c.4960+1G>C
ENST00000339598.5:c.2659+1G>C
ENST00000402415.5:c.2890+1G>C

Variation displays